Compliance Policy Guide Sec. 540.700 Processed and/or Blended Seafood Products (CPG 7108.16); Availability, 71655 [E8-27969]

Download as PDF Federal Register / Vol. 73, No. 228 / Tuesday, November 25, 2008 / Notices presentation will be limited to three minutes. To be placed on the public speaker list, interested parties should contact CAPT Theresa Lawrence in writing (preferably via e-mail), by November 28, 2008. Written Statements: In general, individuals or groups may file written comments with the Task Force. All written comments must be received prior to December 12, 2008 and should be sent to CAPT Theresa Lawrence (preferably by e-mail with ‘‘Task Force Public Comment’’ as the subject line). Individuals needing special assistance should notify CAPT Theresa Lawrence (preferably by e-mail) by November 28, 2008. Dated:November 18, 2008. RADM William C. Vanderwagen, Assistant Secretary for Preparedness and Response, U.S. Department of Health and Human Services. [FR Doc. E8–28013 Filed 11–24–08; 8:45 am] BILLING CODE 4150–37–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2008–D–0588] Compliance Policy Guide Sec. 540.700 Processed and/or Blended Seafood Products (CPG 7108.16); Availability AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration (FDA) is announcing the availability of revised Compliance Policy Guide Sec. 540.700 Processed and/or Blended Seafood Products (CPG 7108.16) (the CPG). The CPG provides guidance for FDA staff on FDA’s labeling requirements for processed and blended seafood products. DATES: Submit written or electronic comments regarding the CPG at any time. Submit written comments on the CPG to the Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. Submit electronic comments to http:// www.regulations.gov. Submit written requests for single copies of the CPG to the Division of Compliance Policy (HFC–230), Office of Enforcement, Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857. Send two self-addressed adhesive labels to assist that office in processing your request, or fax your request to 240–632–6861. See jlentini on PROD1PC65 with NOTICES ADDRESSES: VerDate Aug<31>2005 17:01 Nov 24, 2008 Jkt 217001 the SUPPLEMENTARY INFORMATION section for electronic access to the CPG. FOR FURTHER INFORMATION CONTACT: Catalina Ferre-Hockensmith, Center for Food Safety and Applied Nutrition (HFS–820), Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740, 301– 436–2371. SUPPLEMENTARY INFORMATION: I. Background In the Federal Register of July 26, 1985 (50 FR 30523), FDA made available Compliance Policy Guide 7108.16, which was subsequently renumbered and renamed Compliance Policy Guide Sec. 540.700 Processed and/or Blended Seafood Products (CPG 7108.16). FDA has revised the CPG. The CPG provides guidance for FDA staff on FDA’s labeling requirements for processed and blended seafood products. The CPG also contains information that may be useful to the regulated industry and to the public. FDA is issuing the revisions to the CPG as Level 2 guidance under FDA’s good guidance practices regulation (21 CFR 10.115). Consistent with FDA’s good guidance practices regulation, the agency will accept comments on the CPG at any time. The CPG represents the agency’s current thinking on this topic. It does not create or confer any rights for or on any person and does not operate to bind FDA or the public. An alternate approach may be used if such approach satisfies the requirements of the applicable statutes and regulations. II. Comments Interested persons may submit to the Division of Dockets Management (see ADDRESSES) written or electronic comments regarding the document. Submit a single copy of electronic comments or two paper copies of any mailed comments, except that individuals may submit one paper copy. Comments are to be identified with the docket number found in brackets in the heading of this document. Received comments may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday. Please note that on January 15, 2008, the FDA Division of Dockets Management Web site transitioned to the Federal Dockets Management System (FDMS). FDMS is a Government-wide, electronic docket management system. Electronic comments or submissions will be accepted by FDA only through FDMS at http://www.regulations.gov. PO 00000 Frm 00056 Fmt 4703 Sfmt 4703 71655 III. Electronic Access Persons with access to the Internet may obtain the CPG from FDA’s Office of Regulatory Affairs history page. It may be accessed at http://www.fda.gov/ ora/compliance_ref/cpg/cpgfod/cpg540700.html. Dated: November 14, 2008. Michael A. Chappell, Acting Associate Commissioner for Regulatory Affairs. [FR Doc. E8–27969 Filed 11–24–08; 8:45 am] BILLING CODE 4160–01–S DEPARTMENT OF HOMELAND SECURITY Welcome to the DHS Enterprise eRecruitment System Office of the Chief Human Capital Officer, DHS. ACTION: 60-Day Notice and request for comments; Information Collection submission for OMB Review. AGENCY: SUMMARY: The Department of Homeland Security, Office of the Chief Human Capital Officer has submitted the following information collection request (ICR) to the Office of Management and Budget (OMB) for review and clearance in accordance with the Paperwork Reduction Act of 1995 (Pub. L. 104–13, 44 U.S.C. Chapter 35). DATES: Comments are encouraged and will be accepted until January 26, 2009. This process is conducted in accordance with 5 CFR 1320.1. ADDRESSES: Comments and questions about this Information Collection Request should be forwarded to the Office of the Chief Human Capital Officer, Attn: Mabeline Hall for the Department of Homeland Security/ CHCO, 245 Murray Lane SW., Building 410, Washington, DC 20528. FOR FURTHER INFORMATION CONTACT: Mabeline Hall, 202–357–8272 (this is not a toll free number). SUPPLEMENTARY INFORMATION: The Department of Homeland Security (DHS), Office of the Chief Human Capital Officer (OCHCO) is implementing an enterprise eRecruitment system for DHS. The use of an automated recruitment solution is necessary to meet mission critical needs of DHS and comply with the 45-day hiring model under the President’s Management Agenda. Technology-enabled recruitment can deliver both time savings and improved results. Based on an internal inventory of DHS human resource (HR) systems, more than 50 systems are currently used E:\FR\FM\25NON1.SGM 25NON1

Agencies

[Federal Register Volume 73, Number 228 (Tuesday, November 25, 2008)]
[Notices]
[Page 71655]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-27969]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2008-D-0588]


Compliance Policy Guide Sec. 540.700 Processed and/or Blended 
Seafood Products (CPG 7108.16); Availability

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) is announcing the 
availability of revised Compliance Policy Guide Sec. 540.700 Processed 
and/or Blended Seafood Products (CPG 7108.16) (the CPG). The CPG 
provides guidance for FDA staff on FDA's labeling requirements for 
processed and blended seafood products.

DATES: Submit written or electronic comments regarding the CPG at any 
time.

ADDRESSES: Submit written comments on the CPG to the Division of 
Dockets Management (HFA-305), Food and Drug Administration, 5630 
Fishers Lane, rm. 1061, Rockville, MD 20852. Submit electronic comments 
to http://www.regulations.gov. Submit written requests for single 
copies of the CPG to the Division of Compliance Policy (HFC-230), 
Office of Enforcement, Food and Drug Administration, 5600 Fishers Lane, 
Rockville, MD 20857. Send two self-addressed adhesive labels to assist 
that office in processing your request, or fax your request to 240-632-
6861. See the SUPPLEMENTARY INFORMATION section for electronic access 
to the CPG.

FOR FURTHER INFORMATION CONTACT: Catalina Ferre-Hockensmith, Center for 
Food Safety and Applied Nutrition (HFS-820), Food and Drug 
Administration, 5100 Paint Branch Pkwy., College Park, MD 20740, 301-
436-2371.

SUPPLEMENTARY INFORMATION:

I. Background

    In the Federal Register of July 26, 1985 (50 FR 30523), FDA made 
available Compliance Policy Guide 7108.16, which was subsequently 
renumbered and renamed Compliance Policy Guide Sec. 540.700 Processed 
and/or Blended Seafood Products (CPG 7108.16). FDA has revised the CPG. 
The CPG provides guidance for FDA staff on FDA's labeling requirements 
for processed and blended seafood products. The CPG also contains 
information that may be useful to the regulated industry and to the 
public.
    FDA is issuing the revisions to the CPG as Level 2 guidance under 
FDA's good guidance practices regulation (21 CFR 10.115). Consistent 
with FDA's good guidance practices regulation, the agency will accept 
comments on the CPG at any time. The CPG represents the agency's 
current thinking on this topic. It does not create or confer any rights 
for or on any person and does not operate to bind FDA or the public. An 
alternate approach may be used if such approach satisfies the 
requirements of the applicable statutes and regulations.

II. Comments

    Interested persons may submit to the Division of Dockets Management 
(see ADDRESSES) written or electronic comments regarding the document. 
Submit a single copy of electronic comments or two paper copies of any 
mailed comments, except that individuals may submit one paper copy. 
Comments are to be identified with the docket number found in brackets 
in the heading of this document. Received comments may be seen in the 
Division of Dockets Management between 9 a.m. and 4 p.m., Monday 
through Friday.
    Please note that on January 15, 2008, the FDA Division of Dockets 
Management Web site transitioned to the Federal Dockets Management 
System (FDMS). FDMS is a Government-wide, electronic docket management 
system. Electronic comments or submissions will be accepted by FDA only 
through FDMS at http://www.regulations.gov.

III. Electronic Access

    Persons with access to the Internet may obtain the CPG from FDA's 
Office of Regulatory Affairs history page. It may be accessed at http:/
/www.fda.gov/ora/compliance_ref/cpg/cpgfod/cpg540-700.html.

    Dated: November 14, 2008.
Michael A. Chappell,
Acting Associate Commissioner for Regulatory Affairs.
[FR Doc. E8-27969 Filed 11-24-08; 8:45 am]
BILLING CODE 4160-01-S