Foreign Supplier Verification Programs for Importers of Food for Humans and Animals; Extension of Comment Periods, 69602-69603 [2013-27645]

Download as PDF 69602 Federal Register / Vol. 78, No. 224 / Wednesday, November 20, 2013 / Proposed Rules Piaggio Aero Industries S.p.A. Mandatory Service Bulletin No.: 80–0381, Rev. 0, dated May 2, 2013. (2) If the clearance is less than 5 mm on HS LH or RH side during the measurement as required by paragraph (f)(1) of this AD, before further flight, rework the affected elevator to restore the required minimum clearance between the horn of the elevator and the end rib of the horizontal stabilizer following Part B of the Accomplishment Instructions section of Piaggio Aero Industries S.p.A. Mandatory Service Bulletin No.: 80–0381, Rev. 0, dated May 2, 2013. (3) Within 30 days after accomplishment of the measurement as required by paragraph (f)(1) of this AD, report the results to Piaggio Aero Industries S.p.A. following Part C of the Accomplishment Instructions section of Piaggio Aero Industries S.p.A. Mandatory Service Bulletin No.: 80–0381, Rev. 0, dated May 2, 2013. pmangrum on DSK3VPTVN1PROD with PROPOSALS-1 (g) Other FAA AD Provisions The following provisions also apply to this AD: (1) Alternative Methods of Compliance (AMOCs): The Manager, Standards Office, FAA, has the authority to approve AMOCs for this AD, if requested using the procedures found in 14 CFR 39.19. Send information to ATTN: Mike Kiesov, Aerospace Engineer, FAA, Small Airplane Directorate, 901 Locust, Room 301, Kansas City, Missouri 64106; telephone: (816) 329–4144; fax: (816) 329– 4090; email: mike.kiesov@faa.gov. Before using any approved AMOC on any airplane to which the AMOC applies, notify your appropriate principal inspector (PI) in the FAA Flight Standards District Office (FSDO), or lacking a PI, your local FSDO. (2) Airworthy Product: For any requirement in this AD to obtain corrective actions from a manufacturer or other source, use these actions if they are FAA-approved. Corrective actions are considered FAA-approved if they are approved by the State of Design Authority (or their delegated agent). You are required to assure the product is airworthy before it is returned to service. (3) Reporting Requirements: For any reporting requirement in this AD, a federal agency may not conduct or sponsor, and a person is not required to respond to, nor shall a person be subject to a penalty for failure to comply with a collection of information subject to the requirements of the Paperwork Reduction Act unless that collection of information displays a current valid OMB Control Number. The OMB Control Number for this information collection is 2120–0056. Public reporting for this collection of information is estimated to be approximately 5 minutes per response, including the time for reviewing instructions, completing and reviewing the collection of information. All responses to this collection of information are mandatory. Comments concerning the accuracy of this burden and suggestions for reducing the burden should be directed to the FAA at: 800 Independence Ave. SW., Washington, DC 20591, Attn: Information Collection Clearance Officer, AES–200. VerDate Mar<15>2010 13:59 Nov 19, 2013 Jkt 232001 (h) Related Information Refer to MCAI European Aviation Safety Agency (EASA) AD No. 2013–0239, dated September 30, 2013, for related information. You may examine the MCAI on the Internet at http://www.regulations.gov by searching for and locating it in Docket No. FAA–2013– 0964. For service information related to this AD, contact Piaggio Aero Industries S.p.A— Airworthiness Office, Via Luigi Cibrario, 4– 16154 Genova-Italy; phone: +39 010 6481353; fax: +39 010 6481881; email: Internet: http:// www.piaggioaero.com/#/en/aftersales/ service-support. You may review this referenced service information at the FAA, Small Airplane Directorate, 901 Locust, Kansas City, Missouri 64106. For information on the availability of this material at the FAA, call (816) 329–4148. Issued in Kansas City, Missouri, on November 5, 2013. Earl Lawrence, Manager, Small Airplane Directorate, Aircraft Certification Service. [FR Doc. 2013–27639 Filed 11–19–13; 8:45 am] BILLING CODE 4910–13–P information collection provisions associated with the rule consistent with the comment period for the proposed rule. For the proposed rule published on July 29, 2013 (78 FR 45730), submit either electronic or written comments by January 27, 2014. Submit comments on information collection issues under the Paperwork Reduction Act of 1995 (the PRA) by January 27, 2014 (see the ‘‘Paperwork Reduction Act of 1995’’ section of this document). ADDRESSES: You may submit comments, identified by Docket No. FDA–2011–N– 0143 and/or Regulatory Information Number (RIN) 0910–AG64, by any of the following methods, except that comments on information collection issues under the PRA must be submitted to the Office of Information and Regulatory Affairs, Office of Management and Budget (OMB) (see the ‘‘Paperwork Reduction Act of 1995’’ section of this document). DATES: Electronic Submissions DEPARTMENT OF HEALTH AND HUMAN SERVICES 21 CFR Part 1 Submit electronic comments in the following way: • Federal eRulemaking Portal: http:// www.regulations.gov. Follow the instructions for submitting comments. [Docket No. FDA–2011–N–0143] Written Submissions Food and Drug Administration RIN 0910–AG64 Foreign Supplier Verification Programs for Importers of Food for Humans and Animals; Extension of Comment Periods AGENCY: Food and Drug Administration, HHS. Proposed rule; extension of comment period for the proposed rule and for its information collection provisions. ACTION: The Food and Drug Administration (FDA or we) is extending the comment period for the proposed rule, and for the information collection related to the proposed rule entitled ‘‘Foreign Supplier Verification Programs for Importers of Food for Humans and Animals’’ that appeared in the Federal Register of July 29, 2013. We are taking this action in response to requests for an extension to allow interested persons an opportunity to consider the interrelationship between this proposed rule and the proposed rule announced in October 2013 entitled ‘‘Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food for Animals.’’ We also are taking this action to keep the comment period for the SUMMARY: PO 00000 Frm 00009 Fmt 4702 Sfmt 4702 Submit written submissions in the following ways: • Mail/Hand delivery/Courier (for paper or CD–ROM submissions): Division of Dockets Management (HFA– 305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. Instructions: All submissions received must include the Agency name, Docket No. FDA–2011–N–0143, and RIN 0910– AG64 for this rulemaking. All comments received may be posted without change to http://www.regulations.gov, including any personal information provided. For additional information on submitting comments, see the ‘‘Request for Comments’’ heading of the SUPPLEMENTARY INFORMATION section of this document. Docket: For access to the docket to read background documents or comments received, go to http:// www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ‘‘Search’’ box and follow the prompts and/or go to the Division of Dockets Management, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. FOR FURTHER INFORMATION CONTACT: With regard to the proposed rule: Brian Pendleton, Office of Policy, Food and Drug Administration, 10903 New E:\FR\FM\20NOP1.SGM 20NOP1 Federal Register / Vol. 78, No. 224 / Wednesday, November 20, 2013 / Proposed Rules Hampshire Ave., Silver Spring, MD 20993–0002, 301–796–4614. With regard to the information collection: Domini Bean, Office of Information Management, Food and Drug Administration, 1350 Piccard Dr., PI50–400T, Rockville, MD 20850, Domini.Bean@fda.hhs.gov. SUPPLEMENTARY INFORMATION: pmangrum on DSK3VPTVN1PROD with PROPOSALS-1 I. Background In the Federal Register of July 29, 2013 (78 FR 45730), we published a proposed rule entitled ‘‘Foreign Supplier Verification Programs for Importers of Food for Humans and Animals’’ with a 120-day comment period on the provisions of the proposed rule and on the information collection provisions that are subject to review by OMB under the PRA (44 U.S.C. 3501–3520). FDA has received requests for an extension of the comment period on the proposed rule to allow interested persons an opportunity to consider the interrelationship between this proposed rule and the proposed rule entitled ‘‘Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food for Animals’’ (78 FR 64736, October 29, 2013). FDA has considered the requests and is granting a 60-day extension of the comment period for the ‘‘Foreign Supplier Verification Programs for Importers of Food for Humans and Animals’’ proposed rule to allow interested persons an opportunity to consider the interrelationships between the proposed rules. We also are extending the comment period for the information collection provisions for 60 days to make the comment period for the information collection provisions the same as the comment period for the provisions of the proposed rule. To clarify, FDA is requesting comment on all issues raised by the proposed rule. II. Paperwork Reduction Act of 1995 Interested persons may either submit electronic comments regarding the information collection to oira_ submission@omb.eop.gov or fax written comments to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer, FAX: 202–395–7285. All comments should be identified with the title ‘‘Foreign Supplier Verification Programs for Importers of Food for Humans and Animals.’’ III. Request for Comments Interested persons may submit either electronic comments regarding the proposed rule to http:// www.regulations.gov or written comments to the Division of Dockets VerDate Mar<15>2010 13:59 Nov 19, 2013 Jkt 232001 Management (see ADDRESSES). It is only necessary to send one set of comments. Identify comments 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, and will be posted to the docket at http:// www.regulations.gov. Dated: November 13, 2013. Leslie Kux, Assistant Commissioner for Policy. [FR Doc. 2013–27645 Filed 11–19–13; 8:45 am] BILLING CODE 4160–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES 69603 by January 27, 2014. Submit comments on information collection issues under the Paperwork Reduction Act of 1995 (the PRA) by January 27, 2014 (see the ‘‘Paperwork Reduction Act of 1995’’ section of this document). ADDRESSES: You may submit comments, identified by Docket No. FDA–2011–N– 0146 and/or Regulatory Information Number (RIN) 0910–AG66, by any of the following methods, except that comments on information collection issues under the PRA must be submitted to the Office of Information and Regulatory Affairs, Office of Management and Budget (OMB) (see the ‘‘Paperwork Reduction Act of 1995’’ section of this document). Electronic Submissions [Docket No. FDA–2011–N–0146] Submit electronic comments in the following way: • Federal eRulemaking Portal: http:// www.regulations.gov. Follow the instructions for submitting comments. RIN 0910–AG66 Written Submissions Accreditation of Third-Party Auditors/ Certification Bodies To Conduct Food Safety Audits and To Issue Certifications; Extension of Comment Periods Submit written submissions in the following ways: • Mail/Hand delivery/Courier (for paper or CD–ROM submissions): Division of Dockets Management (HFA– 305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. Instructions: All submissions received must include the Agency name, Docket No. FDA–2011–N–0146, and RIN 0910– AG66 for this rulemaking. All comments received may be posted without change to http://www.regulations.gov, including any personal information provided. For additional information on submitting comments, see the ‘‘Request for Comments’’ heading of the SUPPLEMENTARY INFORMATION section of this document. Docket: For access to the docket to read background documents or comments received, go to http:// www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ‘‘Search’’ box and follow the prompts and/or go to the Division of Dockets Management, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. FOR FURTHER INFORMATION CONTACT: With regard to the proposed rule: Charlotte Christin, Center for Food Safety and Applied Nutrition, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 32, Rm. 4234, Silver Spring, MD 20993–0002, 240– 402–3708. With regard to the information collection: Domini Bean, Office of Information Management, Food and Food and Drug Administration 21 CFR Parts 1 and 16 AGENCY: Food and Drug Administration, HHS. Proposed rule; extension of comment period for the proposed rule and for its information collection provisions. ACTION: The Food and Drug Administration (FDA or we) is extending the comment period for the proposed rule, and for the information collection related to the proposed rule entitled ‘‘Accreditation of Third-Party Auditors/Certification Bodies to Conduct Food Safety Audits and to Issue Certifications’’ that appeared in the Federal Register of July 29, 2013. We are taking this action in response to requests for an extension to allow interested persons an opportunity to consider the interrelationship between this proposed rule and the proposed rule announced in October 2013 entitled ‘‘Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food for Animals.’’ We also are taking this action to keep the comment period for the information collection provisions associated with the rule consistent with the comment period for the proposed rule. SUMMARY: For the proposed rule published on July 29, 2013 (78 FR 45782), submit either electronic or written comments DATES: PO 00000 Frm 00010 Fmt 4702 Sfmt 4702 E:\FR\FM\20NOP1.SGM 20NOP1

Agencies

[Federal Register Volume 78, Number 224 (Wednesday, November 20, 2013)]
[Proposed Rules]
[Pages 69602-69603]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-27645]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 1

[Docket No. FDA-2011-N-0143]
RIN 0910-AG64


Foreign Supplier Verification Programs for Importers of Food for 
Humans and Animals; Extension of Comment Periods

AGENCY: Food and Drug Administration, HHS.

ACTION: Proposed rule; extension of comment period for the proposed 
rule and for its information collection provisions.

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

SUMMARY: The Food and Drug Administration (FDA or we) is extending the 
comment period for the proposed rule, and for the information 
collection related to the proposed rule entitled ``Foreign Supplier 
Verification Programs for Importers of Food for Humans and Animals'' 
that appeared in the Federal Register of July 29, 2013. We are taking 
this action in response to requests for an extension to allow 
interested persons an opportunity to consider the interrelationship 
between this proposed rule and the proposed rule announced in October 
2013 entitled ``Current Good Manufacturing Practice and Hazard Analysis 
and Risk-Based Preventive Controls for Food for Animals.'' We also are 
taking this action to keep the comment period for the information 
collection provisions associated with the rule consistent with the 
comment period for the proposed rule.

DATES: For the proposed rule published on July 29, 2013 (78 FR 45730), 
submit either electronic or written comments by January 27, 2014. 
Submit comments on information collection issues under the Paperwork 
Reduction Act of 1995 (the PRA) by January 27, 2014 (see the 
``Paperwork Reduction Act of 1995'' section of this document).

ADDRESSES: You may submit comments, identified by Docket No. FDA-2011-
N-0143 and/or Regulatory Information Number (RIN) 0910-AG64, by any of 
the following methods, except that comments on information collection 
issues under the PRA must be submitted to the Office of Information and 
Regulatory Affairs, Office of Management and Budget (OMB) (see the 
``Paperwork Reduction Act of 1995'' section of this document).

Electronic Submissions

    Submit electronic comments in the following way:
     Federal eRulemaking Portal: http://www.regulations.gov. 
Follow the instructions for submitting comments.

Written Submissions

    Submit written submissions in the following ways:
     Mail/Hand delivery/Courier (for paper or CD-ROM 
submissions): Division of Dockets Management (HFA-305), Food and Drug 
Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
    Instructions: All submissions received must include the Agency 
name, Docket No. FDA-2011-N-0143, and RIN 0910-AG64 for this 
rulemaking. All comments received may be posted without change to 
http://www.regulations.gov, including any personal information 
provided. For additional information on submitting comments, see the 
``Request for Comments'' heading of the SUPPLEMENTARY INFORMATION 
section of this document.
    Docket: For access to the docket to read background documents or 
comments received, go to http://www.regulations.gov and insert the 
docket number, found in brackets in the heading of this document, into 
the ``Search'' box and follow the prompts and/or go to the Division of 
Dockets Management, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.

FOR FURTHER INFORMATION CONTACT: 
    With regard to the proposed rule: Brian Pendleton, Office of 
Policy, Food and Drug Administration, 10903 New

[[Page 69603]]

Hampshire Ave., Silver Spring, MD 20993-0002, 301-796-4614.
    With regard to the information collection: Domini Bean, Office of 
Information Management, Food and Drug Administration, 1350 Piccard Dr., 
PI50-400T, Rockville, MD 20850, Domini.Bean@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: 

I. Background

    In the Federal Register of July 29, 2013 (78 FR 45730), we 
published a proposed rule entitled ``Foreign Supplier Verification 
Programs for Importers of Food for Humans and Animals'' with a 120-day 
comment period on the provisions of the proposed rule and on the 
information collection provisions that are subject to review by OMB 
under the PRA (44 U.S.C. 3501-3520).
    FDA has received requests for an extension of the comment period on 
the proposed rule to allow interested persons an opportunity to 
consider the interrelationship between this proposed rule and the 
proposed rule entitled ``Current Good Manufacturing Practice and Hazard 
Analysis and Risk-Based Preventive Controls for Food for Animals'' (78 
FR 64736, October 29, 2013). FDA has considered the requests and is 
granting a 60-day extension of the comment period for the ``Foreign 
Supplier Verification Programs for Importers of Food for Humans and 
Animals'' proposed rule to allow interested persons an opportunity to 
consider the interrelationships between the proposed rules. We also are 
extending the comment period for the information collection provisions 
for 60 days to make the comment period for the information collection 
provisions the same as the comment period for the provisions of the 
proposed rule. To clarify, FDA is requesting comment on all issues 
raised by the proposed rule.

II. Paperwork Reduction Act of 1995

    Interested persons may either submit electronic comments regarding 
the information collection to oira_submission@omb.eop.gov or fax 
written comments to the Office of Information and Regulatory Affairs, 
OMB, Attn: FDA Desk Officer, FAX: 202-395-7285. All comments should be 
identified with the title ``Foreign Supplier Verification Programs for 
Importers of Food for Humans and Animals.''

III. Request for Comments

    Interested persons may submit either electronic comments regarding 
the proposed rule to http://www.regulations.gov or written comments to 
the Division of Dockets Management (see ADDRESSES). It is only 
necessary to send one set of comments. Identify comments 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, and will be posted to 
the docket at http://www.regulations.gov.

    Dated: November 13, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013-27645 Filed 11-19-13; 8:45 am]
BILLING CODE 4160-01-P