Food and Drug Administration, HHS.
The Food and Drug Administration (FDA) is announcing the availability of a new subchapter of the Regulatory Procedures Manual. The new subchapter is entitled “Secured Storage.” This subchapter has been provided to FDA's field offices to provide operational procedures for identifying those importers who should be referred to the U.S. Customs Service (U.S. Customs) so that U.S. Customs can require those importers to place their imported foods into secured storage under the control of U.S. Customs pending a decision by FDA of their admissibility. The subchapter is located in Chapter 9 of FDA's Regulatory Procedures Manual.
Submit written comments at any time.
Submit written requests for single copies of the subchapter entitled “Secured Storage” 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.
Submit written comments on the subchapter to the Dockets Management Branch (HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20857. See the SUPPLEMENTARY INFORMATION section for electronic access to the subchapter.Start Further Info
FOR 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 Information
On July 3, 1999, the President announced an initiative to ensure the safety of imported food by directing the Secretary of the Department of Health and Human Services (DHHS) and the Secretary of the Treasury to develop new operational procedures to protect the public health. The initiative is geared to optimize the statutory authorities and resources available to the FDA, DHHS, and the U.S. Customs, Department of the 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 prevent distribution of imported unsafe food by requiring importers with a history of illegal distribution, misrepresentation, or substitution to hold future shipments in secure storage facilities until specifically released by FDA. The subchapter now being made available 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 the FDA's policy for Level 2 guidance documents as set out in the agency's good guidance practices, published in the Federal Register of September 19, 2000 (65 FR 56468).
Interested persons may, at any time, submit written comments to the Dockets Management Branch (address above) regarding this new 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 the brackets in the heading of this document. A copy of the subchapter and any 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 a copy of this subchapter at http://www.fda.gov/ora.Start Signature
Dated: January 12, 2001.
Dennis E. Baker,
Associate Commissioner for Regulatory Affairs.
[FR Doc. 01-1700 Filed 1-17-01; 11:07 am]
BILLING CODE 4160-01-F