Veterinary Feed Directive; Extension of Comment Period, 36588 [2010-15561]

Download as PDF 36588 Federal Register / Vol. 75, No. 123 / Monday, June 28, 2010 / Proposed Rules The FAA’s authority to issue rules regarding aviation safety is found in Title 49 of the U.S. Code. Subtitle 1, section 106 describes the authority of the FAA Administrator. Subtitle VII, Aviation Programs, describes in more detail the scope of the agency’s authority. This rulemaking is promulgated under the authority described in subtitle VII, part A, subpart I, section 40103. Under that section, the FAA is charged with prescribing regulations to assign the use of airspace necessary to ensure the safety of aircraft and the efficient use of airspace. This regulation is within the scope of that authority as it would remove controlled airspace at Chillicotte Municipal Airport, Chillicotte, MO. List of Subjects in 14 CFR Part 71 Airspace, Incorporation by reference, Navigation (Air). The Proposed Amendment In consideration of the foregoing, the Federal Aviation Administration proposes to amend 14 CFR part 71 as follows: PART 71—DESIGNATION OF CLASS A, B, C, D, AND E AIRSPACE AREAS; AIR TRAFFIC SERVICE ROUTES; AND REPORTING POINTS 1. The authority citation for part 71 continues to read as follows: Authority: 49 U.S.C. 106(g); 40103, 40113, 40120; E.O. 10854, 24 FR 9565, 3 CFR, 1959– 1963 Comp., p. 389. § 71.1 [Amended] 2. The incorporation by reference in 14 CFR 71.1 of FAA Order 7400.9T, Airspace Designations and Reporting Points, signed August 27, 2009, and effective September 15, 2009, is amended as follows: Paragraph 6002 Class E Airspace designated as surface areas. * * * jlentini on DSKJ8SOYB1PROD with PROPOSALS ACE MO E2 * * Chillicotte, MO [Removed] Issued in Fort Worth, TX, on June 16, 2010. Anthony D. Roetzel, Manager, Operations Support Group, ATO Central Service Center. [FR Doc. 2010–15680 Filed 6–25–10; 8:45 am] BILLING CODE 4901–13–P VerDate Mar<15>2010 16:02 Jun 25, 2010 Jkt 220001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Parts 510, 514, and 558 [Docket No. FDA–2010–N–0155] Veterinary Feed Directive; Extension of Comment Period AGENCY: Food and Drug Administration, HHS. Advance notice of proposed rulemaking; extension of comment period. ACTION: The Food and Drug Administration (FDA) is extending to August 27, 2010, the comment period for the advance notice of proposed rulemaking (ANPRM) that appeared in the Federal Register of March 29, 2010 (75 FR 15387). In the ANPRM, FDA requested comments on the need for improvements to the veterinary feed directive (VFD) regulation. The agency is taking this action in response to requests for an extension to allow interested persons additional time to submit comments. DATES: Submit either electronic or written comments by August 27, 2010. ADDRESSES: You may submit comments, identified by Docket No. FDA–2010–N– 0155, by any of the following methods: Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: https:// www.regulations.gov. Follow the instructions for submitting comments. Written Submissions Submit written submissions in the following ways: • FAX: 301–827–6870. • Mail/Hand delivery/Courier (for paper, disk, 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 and docket number for this rulemaking. All comments received may be posted without change to https:// www.regulations.gov, including any personal information provided. For additional information on submitting comments, see the ‘‘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 https:// www.regulations.gov and insert the docket number, found in brackets in the SUMMARY: PO 00000 Frm 00012 Fmt 4702 Sfmt 9990 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: Neal Bataller, Center for Veterinary Medicine (HFV–230), Food and Drug Administration, 7500 Standish Pl., Rockville, MD 20855, 240–276–9201, email: Neal.Bataller@fda.hhs.gov. SUPPLEMENTARY INFORMATION: I. Background In the Federal Register of March 29, 2010 (75 FR 15387), FDA published an ANPRM with a 90-day comment period to request comments on the need for improvements to the VFD regulation. The agency has received requests for a 60-day extension of the comment period for the ANPRM. The requests conveyed concern that the current 90day comment period does not allow sufficient time to develop a meaningful or thoughtful response to the ANPRM. FDA has considered the requests and is extending the comment period for the ANPRM for 60 days, until August 27, 2010. The agency believes that a 60-day extension allows adequate time for interested persons to submit comments without significantly delaying rulemaking on these important issues. II. Request for Comments Interested persons may submit to the Division of Dockets Management (see ADDRESSES) either electronic or written comments regarding this document. It is only necessary to send one set of comments. It is no longer necessary to send two copies of mailed 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. Dated: June 22, 2010. Leslie Kux, Acting Assistant Commissioner for Policy. [FR Doc. 2010–15561 Filed 6–25–10; 8:45 am] BILLING CODE 4160–01–S E:\FR\FM\28JNP1.SGM 28JNP1

Agencies

[Federal Register Volume 75, Number 123 (Monday, June 28, 2010)]
[Proposed Rules]
[Page 36588]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-15561]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Parts 510, 514, and 558

[Docket No. FDA-2010-N-0155]


Veterinary Feed Directive; Extension of Comment Period

AGENCY:  Food and Drug Administration, HHS.

ACTION:  Advance notice of proposed rulemaking; extension of comment 
period.

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SUMMARY:  The Food and Drug Administration (FDA) is extending to August 
27, 2010, the comment period for the advance notice of proposed 
rulemaking (ANPRM) that appeared in the Federal Register of March 29, 
2010 (75 FR 15387). In the ANPRM, FDA requested comments on the need 
for improvements to the veterinary feed directive (VFD) regulation. The 
agency is taking this action in response to requests for an extension 
to allow interested persons additional time to submit comments.

DATES:  Submit either electronic or written comments by August 27, 
2010.

ADDRESSES:  You may submit comments, identified by Docket No. FDA-2010-
N-0155, by any of the following methods:
Electronic Submissions
    Submit electronic comments in the following way:
     Federal eRulemaking Portal: https://www.regulations.gov. 
Follow the instructions for submitting comments.
Written Submissions
    Submit written submissions in the following ways:
     FAX: 301-827-6870.
     Mail/Hand delivery/Courier (for paper, disk, 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 
and docket number for this rulemaking. All comments received may be 
posted without change to https://www.regulations.gov, including any 
personal information provided. For additional information on submitting 
comments, see the ``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 https://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: Neal Bataller, Center for Veterinary 
Medicine (HFV-230), Food and Drug Administration, 7500 Standish Pl., 
Rockville, MD 20855, 240-276-9201, e-mail: Neal.Bataller@fda.hhs.gov.

SUPPLEMENTARY INFORMATION:

I. Background

    In the Federal Register of March 29, 2010 (75 FR 15387), FDA 
published an ANPRM with a 90-day comment period to request comments on 
the need for improvements to the VFD regulation.
    The agency has received requests for a 60-day extension of the 
comment period for the ANPRM. The requests conveyed concern that the 
current 90-day comment period does not allow sufficient time to develop 
a meaningful or thoughtful response to the ANPRM.
    FDA has considered the requests and is extending the comment period 
for the ANPRM for 60 days, until August 27, 2010. The agency believes 
that a 60-day extension allows adequate time for interested persons to 
submit comments without significantly delaying rulemaking on these 
important issues.

II. Request for Comments

    Interested persons may submit to the Division of Dockets Management 
(see ADDRESSES) either electronic or written comments regarding this 
document. It is only necessary to send one set of comments. It is no 
longer necessary to send two copies of mailed 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.

    Dated: June 22, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010-15561 Filed 6-25-10; 8:45 am]
BILLING CODE 4160-01-S
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