[Federal Register Volume 68, Number 123 (Thursday, June 26, 2003)]
[Notices]
[Pages 38065-38066]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 03-16110]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 03N-0066]


Agency Information Collection Activities; Announcement of OMB 
Approval; Inspection by Accredited Persons Program Under the Medical 
Device User Fee and Modernization Act of 2002

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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

SUMMARY: The Food and Drug Administration (FDA) is announcing that a 
collection of information entitled ``Inspection by Accredited Persons 
Program Under the Medical Device User Fee and Modernization Act of 
2002'' has been approved by the Office of Management and Budget (OMB) 
under the Paperwork Reduction Act of 1995.

FOR FURTHER INFORMATION CONTACT: Peggy Robbins, Office of Management 
Programs (HFA-250), Food and Drug Administration, 5600 Fishers Lane, 
Rockville, MD 20857, 301-827-1223.

SUPPLEMENTARY INFORMATION: In the Federal Register of April 28, 2003 
(68 FR 22388), 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,

[[Page 38066]]

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 0910-0510. The approval expires on 
September 30, 2003. A copy of the supporting statement for this 
information collection is available on the Internet at http://www.fda.gov/ohrms/dockets.

    Dated: June 19, 2003.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 03-16110 Filed 6-25-03; 8:45 am]
BILLING CODE 4160-01-S