Agency information collection activities: Reporting and recordkeeping requirements,

[Federal Register: May 2, 2002 (Volume 67, Number 85)]

[Notices]

[Page 22089]

From the Federal Register Online via GPO Access [wais.access.gpo.gov]

[DOCID:fr02my02-87]

[[Page 22089]]

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 01N-0231]

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.

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 November 5, 2001 (66 FR 55942), 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 March 31, 2003. A copy of the supporting statement for this information collection is available on the Internet at http://www.fda.gov/ohrms/dockets.

Dated: April 23, 2002. Margaret M. Dotzel, Associate Commissioner for Policy.

[FR Doc. 02-10791Filed5-1-02; 8:45 am]

BILLING CODE: 4160-01-S