[Federal Register Volume 70, Number 109 (Wednesday, June 8, 2005)]
[Notices]
[Pages 33474-33478]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 05-11165]


-----------------------------------------------------------------------

ENVIRONMENTAL PROTECTION AGENCY

[OPP-2005-0131; FRL-7715-5]


Ferric Sodium EDTA; Notice of Filing a Pesticide Petition to 
Establish a Tolerance for a Certain Pesticide Chemical in or on Food

AGENCY: Environmental Protection Agency (EPA).

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: This notice announces the initial filing of a pesticide 
petition

[[Page 33475]]

proposing the establishment of regulations for residues of a certain 
pesticide chemical in or on various food commodities.

DATES: Comments, identified by docket identification (ID) number OPP-
2005-0131, must be received on or before July 8, 2005.

ADDRESSES: Comments may be submitted electronically, by mail, or 
through hand delivery/courier. Follow the detailed instructions as 
provided in Unit I. of the SUPPLEMENTARY INFORMATION.

FOR FURTHER INFORMATION CONTACT: Todd Peterson, Biopesticides and 
Pollution Prevention Division (7511C), Office of Pesticide Programs, 
Environmental Protection Agency, 1200 Pennsylvania Ave., NW., 
Washington, DC 20460-0001; telephone number: (703) 308-7224; e-mail 
address: [email protected].

SUPPLEMENTARY INFORMATION:

I. General Information

A. Does this Action Apply to Me?

     You may be potentially affected by this action if you an 
agricultural producer, food manufacturer, or pesticide manufacturer. 
Potentially affected entities may include, but are not limited to:
     Crop production (NAICS 111)
     Animal production (NAICS 112)
     Food manufacturing (NAICS 311)
     Pesticide manufacturing (NAICS 32532)
    This listing is not intended to be exhaustive, but rather provides 
a guide for readers regarding entities likely to be affected by this 
action. Other types of entities not listed in this unit could also be 
affected. The North American Industrial Classification System (NAICS) 
codes have been provided to assist you and others in determining 
whether this action might apply to certain entities. If you have any 
questions regarding the applicability of this action to a particular 
entity, consult the person listed under FOR FURTHER INFORMATION 
CONTACT.

B. How Can I Get Copies of this Document and Other Related Information?

    1. Docket. EPA has established an official public docket for this 
action under docket identification (ID) number OPP-2005-0131. The 
official public docket consists of the documents specifically 
referenced in this action, any public comments received, and other 
information related to this action. Although, a part of the official 
docket, the public docket does not include Confidential Business 
Information (CBI) or other information whose disclosure is restricted 
by statute. The official public docket is the collection of materials 
that is available for public viewing at the Public Information and 
Records Integrity Branch (PIRIB), Rm. 119, Crystal Mall 2, 
1801 S. Bell St., Arlington, VA. This docket facility is open from 8:30 
a.m. to 4 p.m., Monday through Friday, excluding legal holidays. The 
docket telephone number is (703) 305-5805.
    2. Electronic access. You may access this Federal Register document 
electronically through the EPA Internet under the ``Federal Register'' 
listings at http://www.epa.gov/fedrgstr/.
     An electronic version of the public docket is available through 
EPA's electronic public docket and comment system, EPA Dockets. You may 
use EPA Dockets at http://www.epa.gov/edocket/ to submit or view public 
comments, access the index listing of the contents of the official 
public docket, and to access those documents in the public docket that 
are available electronically. Although, not all docket materials may be 
available electronically, you may still access any of the publicly 
available docket materials through the docket facility identified in 
Unit I.B.1. Once in the system, select `` search,'' then key in the 
appropriate docket ID number.
     Certain types of information will not be placed in the EPA 
Dockets. Information claimed as CBI and other information whose 
disclosure is restricted by statute, which is not included in the 
official public docket, will not be available for public viewing in 
EPA's electronic public docket. EPA's policy is that copyrighted 
material will not be placed in EPA's electronic public docket but will 
be available only in printed, paper form in the official public docket. 
To the extent feasible, publicly available docket materials will be 
made available in EPA's electronic public docket. When a document is 
selected from the index list in EPA Dockets, the system will identify 
whether the document is available for viewing in EPA's electronic 
public docket. Although, not all docket materials may be available 
electronically, you may still access any of the publicly available 
docket materials through the docket facility identified in Unit I.B.1. 
EPA intends to work towards providing electronic access to all of the 
publicly available docket materials through EPA's electronic public 
docket.
     For public commenters, it is important to note that EPA's policy 
is that public comments, whether submitted electronically or on paper, 
will be made available for public viewing in EPA's electronic public 
docket as EPA receives them and without change, unless the comment 
contains copyrighted material, CBI, or other information whose 
disclosure is restricted by statute. When EPA identifies a comment 
containing copyrighted material, EPA will provide a reference to that 
material in the version of the comment that is placed in EPA's 
electronic public docket. The entire printed comment, including the 
copyrighted material, will be available in the public docket.
     Public comments submitted on computer disks that are mailed or 
delivered to the docket will be transferred to EPA's electronic public 
docket. Public comments that are mailed or delivered to the docket will 
be scanned and placed in EPA's electronic public docket. Where 
practical, physical objects will be photographed, and the photograph 
will be placed in EPA's electronic public docket along with a brief 
description written by the docket staff.

C. How and to Whom Do I Submit Comments?

     You may submit comments electronically, by mail, or through hand 
delivery/courier. To ensure proper receipt by EPA, identify the 
appropriate docket ID number in the subject line on the first page of 
your comment. Please ensure that your comments are submitted within the 
specified comment period. Comments received after the close of the 
comment period will be marked ``late.'' EPA is not required to consider 
these late comments. If you wish to submit CBI or information that is 
otherwise protected by statute, please follow the instructions in Unit 
I.D. Do not use EPA Dockets or e-mail to submit CBI or information 
protected by statute.
    1. Electronically. If you submit an electronic comment as 
prescribed in this unit, EPA recommends that you include your name, 
mailing address, and an e-mail address or other contact information in 
the body of your comment. Also, include this contact information on the 
outside of any disk or CD ROM you submit, and in any cover letter 
accompanying the disk or CD ROM. This ensures that you can be 
identified as the submitter of the comment and allows EPA to contact 
you in case EPA cannot read your comment due to technical difficulties 
or needs further information on the substance of your comment. EPA's 
policy is that EPA will not edit your comment, and any identifying or 
contact information provided in the body of a comment will be included 
as part of the comment that is placed in the official public docket,

[[Page 33476]]

and made available in EPA's electronic public docket. If EPA cannot 
read your comment due to technical difficulties and cannot contact you 
for clarification, EPA may not be able to consider your comment.
    i. EPA Dockets. Your use of EPA's electronic public docket to 
submit comments to EPA electronically is EPA's preferred method for 
receiving comments. Go directly to EPA Dockets at http://www.epa.gov/edocket/, and follow the online instructions for submitting comments. 
Once in the system, select ``search,'' and then key in docket ID number 
OPP-2005-0131. The system is an ``anonymous access'' system, which 
means EPA will not know your identity, e-mail address, or other contact 
information unless you provide it in the body of your comment.
    ii. E-mail. Comments may be sent by e-mail to [email protected], 
Attention: Docket ID number OPP-2005-0131. In contrast to EPA's 
electronic public docket, EPA's e-mail system is not an ``anonymous 
access'' system. If you send an e-mail comment directly to the docket 
without going through EPA's electronic public docket, EPA's e-mail 
system automatically captures your e-mail address. E-mail addresses 
that are automatically captured by EPA's e-mail system are included as 
part of the comment that is placed in the official public docket, and 
made available in EPA's electronic public docket.
    iii. Disk or CD ROM. You may submit comments on a disk or CD ROM 
that you mail to the mailing address identified in Unit I.C.2. These 
electronic submissions will be accepted in WordPerfect or ASCII file 
format. Avoid the use of special characters and any form of encryption.
    2. By mail. Send your comments to: Public Information and Records 
Integrity Branch (PIRIB) (7502C), Office of Pesticide Programs (OPP), 
Environmental Protection Agency, 1200 Pennsylvania Ave., NW., 
Washington, DC 20460-0001, Attention: Docket ID number OPP-2005-0131.
    3. By hand delivery or courier. Deliver your comments to: Public 
Information and Records Integrity Branch (PIRIB), Office of Pesticide 
Programs (OPP), Environmental Protection Agency, Rm. 119, Crystal Mall 
2, 1801 S. Bell St., Arlington, VA, Attention: Docket ID 
number OPP-2005-0131. Such deliveries are only accepted during the 
docket's normal hours of operation as identified in Unit I.B.1.

D. How Should I Submit CBI to the Agency?

     Do not submit information that you consider to be CBI 
electronically through EPA's electronic public docket or by e-mail. You 
may claim information that you submit to EPA as CBI by marking any part 
or all of that information as CBI (if you submit CBI on disk or CD ROM, 
mark the outside of the disk or CD ROM as CBI and then identify 
electronically within the disk or CD ROM the specific information that 
is CBI). Information so marked will not be disclosed except in 
accordance with procedures set forth in 40 CFR part 2.
     In addition to one complete version of the comment that includes 
any information claimed as CBI, a copy of the comment that does not 
contain the information claimed as CBI must be submitted for inclusion 
in the public docket and EPA's electronic public docket. If you submit 
the copy that does not contain CBI on disk or CD ROM, mark the outside 
of the disk or CD ROM clearly that it does not contain CBI. Information 
not marked as CBI will be included in the public docket and EPA's 
electronic public docket without prior notice. If you have any 
questions about CBI or the procedures for claiming CBI, please consult 
the person listed under FOR FURTHER INFORMATION CONTACT.

E. What Should I Consider as I Prepare My Comments for EPA?

     You may find the following suggestions helpful for preparing your 
comments:
    1. Explain your views as clearly as possible.
    2. Describe any assumptions that you used.
    3. Provide copies of any technical information and/or data you used 
that support your views.
    4. If you estimate potential burden or costs, explain how you 
arrived at the estimate that you provide.
    5. Provide specific examples to illustrate your concerns.
    6. Make sure to submit your comments by the deadline in this 
notice.
    7. To ensure proper receipt by EPA, be sure to identify the docket 
ID number assigned to this action in the subject line on the first page 
of your response. You may also provide the name, date, and Federal 
Register citation.

II. What Action is the Agency Taking?

     EPA has received a pesticide petition as follows proposing the 
establishment and/or amendment of regulations for residues of a certain 
pesticide chemical in or on various food commodities under section 408 
of the Federal Food, Drug, and Cosmetic Act (FFDCA), 21 U.S.C. 346a. 
EPA has determined that this petition contains data or information 
regarding the elements set forth in FFDCA section 408(d)(2); however, 
EPA has not fully evaluated the sufficiency of the submitted data at 
this time or whether the data support granting of the petition. 
Additional data may be needed before EPA rules on the petition.

List of Subjects

    Environmental protection, Agricultural commodities, Feed additives, 
Food additives, Pesticides and pests, Reporting and recordkeeping 
requirements.

    Dated: May 24, 2005.
Janet L. Andersen,
Director, Biopesticides and Pollution Prevention Division, Office of 
Pesticide Programs.

Summary of Petition

     The petitioner's summary of the pesticide petition is printed 
below as required by FFDCA section 408(d)(3). The summary of the 
petition was prepared by the Woodstream Corporation and represents the 
view of the petitioner. The petition summary announces the availability 
of a description of the analytical methods available to EPA for the 
detection and measurement of the pesticide chemical residues or an 
explanation of why no such method is needed.

 Woodstream Corporation

 PP 5F6899

     EPA has received a pesticide petition (PP 5F6899) from Woodstream 
Corporation, 69 N. Locust Street, Lititz, PA 17543-0327, proposing 
pursuant to section 408(d) of the Federal Food, Drug, and Cosmetic Act 
(FFDCA), 21 U.S.C. 346a(d), to amend 40 CFR part 180 to establish an 
exemption from the requirement of a tolerance for the biochemical 
pesticide ferric sodium EDTA.
     Pursuant to section 408(d)(2)(A)(i) of the FFDCA, as amended, 
Woodstream Corporation has submitted the following summary of 
information, data, and arguments in support of their pesticide 
petition. This summary was prepared by Woodstream Corporation and EPA 
has not fully evaluated the merits of the pesticide petition. The 
summary may have been edited by EPA if the terminology used was 
unclear, the summary contained extraneous material, or the summary 
unintentionally made the reader conclude that the findings reflected

[[Page 33477]]

EPA's position and not the position of the petitioner.

A. Product Name and Proposed Use Practices

     Ferric sodium EDTA (technical grade active ingredient) and slug 
and snail killer (end-use product). Ferric sodium EDTA is a highly 
efficacious replacement for metaldehyde for the control of snails and 
slugs. The proposed end-use product (slug and snail killer) contains 
6.00% active ingredient in a flour-based pellet. All intentionally 
added inert ingredients are exempt from the requirement of a tolerance 
when used in pesticides and are on EPA's List 4. Use sites proposed 
include agricultural crops, turf and ornamentals and home gardens; all 
areas where slugs and snails are a problem. The end-use product is 
applied directly to the soil surface. A draft end-use product label has 
been submitted with the corresponding application for FIFRA section 3 
registration.

B. Product Identity/Chemistry

    1. Identity of the pesticide and corresponding residues. The active 
ingredient, ferric sodium EDTA, is comprised of iron in a sodium EDTA 
chelate. Ferric sodium EDTA is a commodity ingredient used in the 
photographic industry as a bleaching agent, used in agriculture as a 
micronutrient, and used in the chemical industry as a catalyst. Ferric 
sodium EDTA is also currently being evaluated as a way of fortifying 
foods to prevent anemia and iron deficiencies in developing countries. 
Iron is an essential element for nutrition and is listed as GRAS for 
direct addition to food per 21 CFR 184.1375. Sodium EDTA is a common 
chelating agent, which immobilizes metal ions until in an environment 
where they are available for uptake. Sodium EDTA is exempt per 40 CFR 
180.1001 when used in pesticide formulations, and is a direct food 
additive per 21 CFR 172.135.
     Ferric sodium EDTA has been classified as ``Not a biochemical, but 
eligible for a reduced data set'' per the Agency's letter received May 
16, 2001. EPA states the classification is based on the abundance of 
iron in nature, its low toxicity, its use as a nutritional supplement, 
and it slow water solubility.
     The end-use product Snail and Slug Control is formulated in pellet 
form with food attractants (flour-based ingredients). Snails and slugs 
are attracted to and ingest the pellets. When ingested, the iron in 
ferric sodium EDTA is available for uptake into the mollusks gut. 
Normally iron is prevented from passing through the gut barrier; 
however, the formulation of iron with the chelating agent EDTA allows 
for iron to pass the gut barrier. Once passed, the iron partially 
acidifies the mollusks copper-based blood resulting in sickness. The 
mollusk stops feeding and leaves the area.
    2. Magnitude of residue at the time of harvest and method used to 
determine the residue.
    3. A statement of why an analytical method for detecting and 
measuring the levels of the pesticide residue are not needed. An 
analytical method for residues is not applicable. It is expected that, 
when used as proposed, ferric sodium EDTA would not result in residues 
that are of toxicological concern.

C. Mammalian Toxicological Profile

     Studies to evaluate the safety to mammals were conducted on the 
technical grade active ingredient (tgai) and are summarized as follows:
    1. Acute oral toxicity (OPPTS Harmonized Guideline 870.1100): No 
adverse effects were seen in rats that received an oral gavage dose of 
5,000 milligrams/kilogram body weight (mg/kg bwt) of the technical 
grade active ingredient. No rats died during the 14-day observation 
period, and no gross pathological changes were found in organs in the 
thoracic or abdominal cavities at necropsy. A LD50 >5,000 
mg/kg was established.
    2. Acute dermal toxicity (OPPTS Harmonized Guideline 870.1200): No 
adverse effects were seen in rats that received a dermal dose of 5,000 
mg/kg bwt of the technical grade active ingredient. No effects on 
appearance, behavior or body weight were observed in any rats any time 
after exposure. No rats died during the 14-day observation period, and 
no gross pathological changes were found in organs in the thoracic or 
abdominal cavities at necropsy. A LD50 >5,000 mg/kg was 
established.
    3. Acute inhalation toxicity (OPPTS Harmonized Guideline 870.1300). 
No adverse effects were seen in rats that were exposed by inhalation 
for 4 hours to a concentration of 2.05 milligrams/Liter (mg/L) of the 
technical grade active ingredient. No effects on appearance, behavior 
or body weight were observed in any rats any time after exposure. No 
rats died during the 14-day observation period, and no gross 
pathological changes were found in organs in the thoracic or abdominal 
cavities at necropsy. A LD50 >2.05 mg/L was established.
    4. Primary eye irritation (OPPTS Harmonized Guideline 870.2400). In 
an eye irritation study on rabbits, ferric sodium EDTA was classified 
as mildly irritating to the eye. The active ingredient was instilled 
into the right eye of three healthy rabbits. Twenty four hours after 
instillation, conjunctivitis and corneal opacity were observed. 
Conjunctivitis cleared in all test animals by Day 10, and corneal 
opacity persisted in one test animal through Day 21. No iritis was 
observed in any treated eye during the study.
    5. Primary Dermal Irritation (OPPTS Harmonized Guideline 870.2500). 
In a skin irritation study on rabbits, ferric sodium EDTA was 
classified as slightly irritating to the skin. The active ingredient 
was applied to the skin of healthy rabbits for 4 hours. No edema was 
noted at any test site during the study. One hour after test material 
application all treated sites exhibited erythema. All animals were free 
of dermal irritation by 24 hours.
    6. Dermal sensitization (OPPTS Harmonized Guideline 870.2600). In a 
dermal sensitization study on guinea pigs, ferric sodium EDTA was not 
considered to be a contact sensitizer. The active ingredient was 
topically applied to test animals once a week for a 3-week induction 
period, and 28 days after the first induction dose as a challenge dose 
at the highest non-irritation concentration. No positive responses were 
observed.
     A waiver is requested for subchronic, teratogenicity, genotoxicity 
and immunotoxicity data requirements. The active ingredient, ferric 
sodium EDTA, is comprised of iron in a sodium EDTA chelate. Ferric 
sodium EDTA is a commodity ingredient used in the photographic industry 
as a bleaching agent, used in agriculture as a micronutrient, and used 
in the chemical industry as a catalyst. Ferric sodium EDTA is also 
currently being evaluated as a way of fortifying foods to prevent 
anemia and iron deficiencies in developing countries. Iron is an 
essential element for nutrition and is listed as GRAS for direct 
addition to food per 21 CFR 184.1375. Sodium EDTA is a common chelating 
agent, which immobilizes metal ions until in an environment where they 
are available for uptake. Sodium EDTA is exempt per 40 CFR 180.1001 
when used in pesticide formulations, and is a direct food additive per 
21 CFR 172.135.
     A complete literature search was conducted on ferric sodium EDTA, 
its components and related compounds. In a safety assessment of ferric 
sodium EDTA (also referred to as ``iron EDTA'') for Food and Drug 
Administration (FDA) GRAS evaluation, the ingredient is regarded as 
safe for use in foods to

[[Page 33478]]

increase iron bioavailability in human diets (Heimbach et al. 2000).
     The results of toxicity testing and information found in published 
literature indicate there is no risk to human health or the environment 
from ferric sodium EDTA. Both dietary and non-dietary exposures would 
not be expected to pose any quantifiable risk due to a lack of residues 
of toxicological concern.

D. Aggregate Exposure

    1. Dietary exposure--i. Food. Dietary exposure from use of ferric 
sodium EDTA, as proposed, is minimal. Ferric sodium EDTA is intended 
for application to soil surfaces in agricultural crops, turf and 
ornamentals, and home gardens to control slugs and snails. The product 
is not applied directly to fruits, vegetables, or plant surfaces.
     Ferric sodium EDTA is a commodity ingredient used in the 
photographic industry as a bleaching agent, used in agriculture as a 
micronutrient, and used in the chemical industry as a catalyst. Ferric 
sodium EDTA is also currently being evaluated as a way of fortifying 
foods to prevent anemia and iron deficiencies in developing countries. 
The components of ferric sodium EDTA are approved as direct food 
additives by FDA. Acute toxicity studies have shown that ferric sodium 
EDTA is not toxic or irritating to mammals. Further, a published safety 
assessment on ferric sodium EDTA for FDA GRAS evaluation, the 
ingredient is regarded as safe for use in foods to increase iron 
bioavailability in human diets (Heimbach et al. 2000),
     The results of toxicity testing and information found in published 
literature indicate there is no risk to human health or the environment 
from ferric sodium EDTA. Dietary exposures would not be expected to 
pose any quantifiable risk due to a lack of residues of toxicological 
concern.
    ii. Drinking water. Similarly, exposure to humans from residues of 
ferric sodium EDTA in consumed drinking water would be unlikely. 
Potential exposure to surface water would be negligible and exposure to 
drinking water (well or ground water) would be impossible to measure. 
Ferric sodium EDTA is intended for application to soil surfaces in 
agricultural crops, turf and ornamentals, and home gardens to control 
slugs and snails. The product is not applied directly to water.
     The results of toxicity testing and information found in published 
literature indicate there is no risk to human health or the environment 
from ferric sodium EDTA. Drinking water exposures would not be expected 
to pose any quantifiable risk due to a lack of residues of 
toxicological concern.
    2. Non-dietary exposure. The potential for non-dietary exposure to 
the general population, including infants and children, is limited. 
Ferric sodium EDTA is intended for application to soil surfaces in 
agricultural crops, turf and ornamentals, and home gardens to control 
slugs and snails.
     The results of toxicity testing and information found in published 
literature indicate there is no risk to human health or the environment 
from ferric sodium EDTA. Non-dietary exposures would not be expected to 
pose any quantifiable risk due to a lack of residues of toxicological 
concern.

E. Cumulative Exposure

     It is not expected that, when used as proposed, ferric sodium EDTA 
would result in residues that are of toxicological concern. Ferric 
sodium EDTA is a commodity ingredient used in the photographic industry 
as a bleaching agent, used in agriculture as a micronutrient, and used 
in the chemical industry as a catalyst. Ferric sodium EDTA is also 
currently being evaluated as a way of fortifying foods to prevent 
anemia and iron deficiencies in developing countries. The components of 
ferric sodium EDTA are approved as direct food additives by FDA. Acute 
toxicity studies have shown that ferric sodium EDTA is not toxic or 
irritating to mammals. Further, a published safety assessment on ferric 
sodium EDTA for FDA GRAS evaluation, the ingredient is regarded as safe 
for use in foods to increase iron bioavailability in human diets 
(Heimbach et al. 2000).
     Ferric sodium EDTA is intended for application to soil surfaces in 
agricultural crops, turf and ornamentals, and home gardens to control 
slugs and snails. The results of toxicity testing and information found 
in published literature indicate there is no risk to human health or 
the environment from ferric sodium EDTA.

F. Safety Determination

    1. U.S. population. Ferric sodium EDTA is a commodity ingredient 
used in the photographic industry as a bleaching agent, used in 
agriculture as a micronutrient, and used in the chemical industry as a 
catalyst. Ferric sodium EDTA is also currently being evaluated as a way 
of fortifying foods to prevent anemia and iron deficiencies in 
developing countries. The components of ferric sodium EDTA are approved 
as direct food additives by FDA. Acute toxicity studies have shown that 
ferric sodium EDTA is not toxic or irritating to mammals. Further, a 
published safety assessment on ferric sodium EDTA for FDA GRAS 
evaluation, the ingredient is regarded as safe for use in foods to 
increase iron bioavailability in human diets (Heimbach et al. 2000).
     When used as proposed, ferric sodium EDTA would not result in 
residues that are of toxicological concern. Ferric sodium EDTA is 
intended for application to soil surfaces in agricultural crops, turf 
and ornamentals, and home gardens to control slugs and snails. The 
results of toxicity testing and information found in published 
literature indicate there is no risk to human health or the environment 
from ferric sodium EDTA. There is a reasonable certainty of no harm to 
the general U.S. population from exposure to this active ingredient.
    2. Infants and children. As mentioned above, it is not expected 
that, when used as proposed, ferric sodium EDTA would result in 
residues that are of toxicological concern. There is a reasonable 
certainty of no harm for infants and children from exposure to ferric 
sodium EDTA from the proposed uses.

G. Effects on the Immune and Endocrine Systems

     To date there is no evidence to suggest that ferric sodium EDTA 
functions in a manner similar to any known hormone, or that it acts as 
an endocrine disrupter.

H. Existing Tolerances

     There is no EPA tolerance for ferric sodium EDTA.

I. International Tolerances

     A Codex Alimentarium Commission Maximum Residue Level (MRL) is not 
required for ferric sodium EDTA.

[FR Doc. 05-11165 Filed 6-7-05; 8:45 am]
BILLING CODE 6560-50-S