[Federal Register Volume 68, Number 112 (Wednesday, June 11, 2003)]
[Notices]
[Page 34980]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 03-14623]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 02N-0383]


Agency Information Collection Activities; Announcement of OMB 
Approval; Veterinary Adverse Drug Reaction, Lack of Effectiveness, 
Product Defect Report

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is announcing that a 
collection of information entitled ``Veterinary Adverse Drug Reaction, 
Lack of Effectiveness, Product Defect Report'' has been approved by the 
Office of Management and Budget (OMB) under the Paperwork Reduction Act 
of 1995.

FOR FURTHER INFORMATION CONTACT: Denver Presley, Office of Information 
Resources Management (HFA-250), Food and Drug Administration, 5600 
Fishers Lane, Rockville, MD 20857, 301-827-1472.

SUPPLEMENTARY INFORMATION: In the Federal Register of March 7, 2003 (68 
FR 11117), the agency announced that the proposed information 
collection had been submitted to OMB for review and clearance under 44 
U.S.C. 3507. An agency may not conduct or sponsor, and a person is not 
required to respond to, a collection of information unless it displays 
a currently valid OMB control number. OMB has now approved the 
information collection and has assigned OMB control number 0910-0012. 
The approval expires on May 31, 2004.

    Dated: June 4, 2003.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 03-14623 Filed 6-10-03; 8:45 am]
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