Legal Status
Legal Status
Notice
Regulatory Procedures Manual; Chapter 9: Import Operations/Action, Subchapter: Secured Storage; 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 6627
- Page:
- 6627 (1 page)
- Agency/Docket Number:
- Docket No. 01D-0002
- Document Number:
- 01-1700
Document Details
-
Enhanced Content - Table of Contents
This tables of contents is a navigational tool, processed from the headings within the legal text of Federal Register documents. This repetition of headings to form internal navigation links has no substantive legal effect.
Enhanced Content - Table of Contents
-
Enhanced Content - Submit Public Comment
- This feature is not available for this document.
Enhanced Content - Submit Public Comment
-
Enhanced Content - Read Public Comments
- This feature is not available for this document.
Enhanced Content - Read Public Comments
-
Enhanced Content - Sharing
- Shorter Document URL
- https://www.federalregister.gov/d/01-1700 https://www.federalregister.gov/d/01-1700
Enhanced Content - Sharing
-
Enhanced Content - Document Tools
These tools are designed to help you understand the official document better and aid in comparing the online edition to the print edition.
-
These markup elements allow the user to see how the document follows the Document Drafting Handbook that agencies use to create their documents. These can be useful for better understanding how a document is structured but are not part of the published document itself.
Display Non-Printed Markup Elements
Enhanced Content - Document Tools
-
-
Enhanced Content - Developer Tools
This document is available in the following developer friendly formats:
- JSON: Normalized attributes and metadata
- XML: Original full text XML
- MODS: Government Publishing Office metadata
More information and documentation can be found in our developer tools pages.
Enhanced Content - Developer Tools
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 “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.
DATES:
Submit written comments at any time.
ADDRESSES:
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 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 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).
II. Comments
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 SignatureDated: 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