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Notice
Regulatory Procedures Manual; Chapter 9: Import Operations/Action, Subchapter: Communication Concerning Assessment of Civil Monetary Penalties by U.S. Customs Service in Cases Involving Imported Food; Availability
A Notice by the Food and Drug Administration on
Document Details
Information about this document as published in the Federal Register.
- Printed version:
- Publication Date:
- 01/22/2001
- Agencies:
- Food and Drug Administration
- Dates:
- Submit written comments at any time.
- Document Type:
- Notice
- Document Citation:
- 66 FR 6626
- Page:
- 6626 (1 page)
- Agency/Docket Number:
- Docket No. 01D-0001
- Document Number:
- 01-1699
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Published Document
This document has been published in the Federal Register. Use the PDF linked in the document sidebar for the official electronic format.
AGENCY:
Food and Drug Administration, HHS.
ACTION:
Notice.
SUMMARY:
The Food and Drug Administration (FDA) is announcing the availability of a new subchapter of the Regulatory Procedures Manual. The new subchapter is entitled “Communication Concerning Assessment of Civil Monetary Penalties by U.S. Customs Service in Cases Involving Imported Food.” This subchapter has been provided to FDA's field offices to provide procedures for communication with the U.S. Customs Service (U.S. Customs) regarding assessment of civil monetary penalties involving imported foods. The subchapter is located in FDA's Regulatory Procedures Manual.
DATES:
Submit written comments at any time.
ADDRESSES:
Submit written requests for single copies of the subchapter entitled “Communication Concerning Assessment of Civil Monetary Penalties by U.S. Customs Service in Cases Involving Imported Food” to Joseph L. McCallion, Division of Import Operations and Policy (HFC-170), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857. Send one self-addressed adhesive label to assist that office in processing your request. See the SUPPLEMENTARY INFORMATION section for electronic access to the subchapter.
Submit written comments on the subchapter to the Dockets Management Branch (HFA-305), 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
Start Further InfoFOR FURTHER INFORMATION CONTACT:
Joseph L. McCallion, Division of Import Operations and Policy (HFC-170), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-443-6553.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
I. Background
On July 3, 1999, the President announced an initiative to ensure the safety of imported food by directing the Secretary of Health and Human Services (DHHS) and the Secretary of Treasury to develop new operational procedures to protect the public health. The initiative is geared to optimize the statutory authorities and resources available to FDA, DHHS and U.S. Customs, Department of Treasury to protect consumers from unsafe imported foods. The President directed the agencies to target unscrupulous importers who violate the import laws and work to subvert the system by introducing unsafe foods into U.S. markets. Six specific objectives were emphasized in the directive.
On December 11, 1999, the President announced the plan developed by FDA and U.S. Customs in response to the directive of July 3, 1999. One element of the plan was to enhance enforcement by having U.S. Customs assess civil monetary penalties in cooperation with FDA. The subchapter now being announced is setting out the procedures for accomplishing this objective.
The subchapter does not create or confer any rights, privileges, or benefits for, or on, any person and does not operate to bind FDA, U.S. Customs, or the public. The subchapter is being distributed in accordance with FDA's policy for Level 2 guidance documents as set out in the agency's good guidance practices regulation, published in the Federal Register of September 19, 2000 (65 FR 56468).
II. Comments
Interested persons may, at any time, submit written comments to the Dockets Management Branch (address above) regarding this subchapter. Two copies of any comments are to be submitted, except individuals may submit one copy. Comments should be identified with the docket number found in brackets in the heading of this document. A copy of the document and received comments are available for public examination in the Dockets Management Branch between 9 a.m. and 4 p.m., Monday through Friday.
III. Electronic Access
Persons with access to the Internet may obtain copies of the subchapter at http://www.fda.gov/ora.
Start SignatureDated: January 12, 2001.
Dennis E. Baker,
Associate Commissioner for Regulatory Affairs.
[FR Doc. 01-1699 Filed 1-17-01; 11:07 am]
BILLING CODE 4160-01-F