Agency information collection activities: Reporting and recordkeeping requirements,

[Federal Register: October 15, 2001 (Volume 66, Number 199)]

[Notices]

[Page 52417]

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

[DOCID:fr15oc01-49]

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 01N-0046]

Agency Information Collection Activities; Announcement of OMB Approval; Current Good Manufacturing Practice Regulations for Medicated Feeds

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

SUMMARY: The Food and Drug Administration (FDA) is announcing that a collection of information entitled ``Current Good Manufacturing Practice Regulations for Medicated Feeds'' has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995 (the PRA).

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 June 15, 2001 (66 FR 32629), 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 0910-0152. The approval expires on September 30, 2004. A copy of the supporting statement for this information collection is available on the Internet at http://www.fda.gov/ohrms/dockets.

Dated: October 5, 2001. Margaret M. Dotzel, Associate Commissioner for Policy.

[FR Doc. 01-25763Filed10-12-01; 8:45 am]

BILLING CODE 4160-01-S