Food Safety Modernization Act Domestic and Foreign Facility Reinspections, Recall, and Importer Reinspection User Fee Rates for Fiscal Year 2012; Correction, 53478 [2011-21895]

Download as PDF 53478 Federal Register / Vol. 76, No. 166 / Friday, August 26, 2011 / Notices meeting whether you have any financial involvement with manufacturers (or their competitors) of any items or services being discussed. The Committee will deliberate openly on the topics under consideration. Interested persons may observe the deliberations, but the Committee will not hear further comments during this time except at the request of the chairperson. The Committee will also allow a 15-minute open public session for any unscheduled speaker to address issues specific to the topics under consideration. At the conclusion of the day, the members will vote and the Committee will make its recommendation(s) to CMS. III. Registration Instructions CMS’ Coverage and Analysis Group is coordinating meeting registration. While there is no registration fee, individuals must register to attend. You may register online at https://www.cms.gov/apps/ events/upcomingevents. asp?strOrderBy=1&type=3 or by phone by contacting the person listed in the FOR FURTHER INFORMATION CONTACT emcdonald on DSK2BSOYB1PROD with NOTICES section of this notice by the deadline listed in the DATES section of this notice. Please provide your full name (as it appears on your state-issued driver’s license), address, organization, telephone, fax number(s), and e-mail address. You will receive a registration confirmation with instructions for your arrival at the CMS complex or you will be notified the seating capacity has been reached. IV. Security, Building, and Parking Guidelines This meeting will be held in a Federal government building; therefore, Federal security measures are applicable. We recommend that confirmed registrants arrive reasonably early, but no earlier than 45 minutes prior to the start of the meeting, to allow additional time to clear security. Security measures include the following: • Presentation of government-issued photographic identification to the Federal Protective Service or Guard Service personnel. • Inspection of vehicle’s interior and exterior (this includes engine and trunk inspection) at the entrance to the grounds. Parking permits and instructions will be issued after the vehicle inspection. • Inspection, via metal detector or other applicable means of all persons brought entering the building. We note that all items brought into CMS, whether personal or for the purpose of presentation or to support a presentation, are subject to inspection. VerDate Mar<15>2010 19:37 Aug 25, 2011 Jkt 223001 We cannot assume responsibility for coordinating the receipt, transfer, transport, storage, set-up, safety, or timely arrival of any personal belongings or items used for presentation or to support a presentation. 1. On page 45822, in the second column, in the first line, ‘‘$335’’ is corrected to read ‘‘$325’’. 2. On page 45822, in the second column, in ‘‘Table 3—FSMA Fee Schedule for FY 2012,’’ ‘‘$335’’ is corrected to read ‘‘$325’’. Note: Individuals who are not registered in advance will not be permitted to enter the building and will be unable to attend the meeting. The public may not enter the building earlier than 45 minutes prior to the convening of the meeting. All visitors must be escorted in areas other than the lower and first floor levels in the Central Building. Dated: August 19, 2011. Leslie Kux, Acting Assistant Commissioner for Policy. Authority: 5 U.S.C. App. 2, section 10(a). (Catalog of Federal Domestic Assistance Program No. 93.773, Medicare—Hospital Insurance; and Program No. 93.774, Medicare—Supplementary Medical Insurance Program) Dated: August 17, 2011. Patrick Conway, CMS Chief Medical Officer and Director, Office of Clinical Standards and Quality Centers for Medicare & Medicaid Services. [FR Doc. 2011–21708 Filed 8–25–11; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2011–N–0528] Food Safety Modernization Act Domestic and Foreign Facility Reinspections, Recall, and Importer Reinspection User Fee Rates for Fiscal Year 2012; Correction AGENCY: Food and Drug Administration, HHS. ACTION: Notice; correction. The Food and Drug Administration (FDA) is correcting a notice that appeared in the Federal Register of August 1, 2011 (76 FR 45820). The document announced the fiscal year 2012 fee rates for certain domestic and foreign facility reinspections, failure to comply with a recall order, and importer reinspections that are mandated in the FDA Food Safety Modernization Act (FSMA). The document was published with two typographical errors. This document corrects those errors. FOR FURTHER INFORMATION CONTACT: Amy Waltrip, 12420 Parklawn Dr., Rm. 2012, Rockville, MD 20857, 301–796– 8811, e-mail: Amy.Waltrip@fda.hhs.gov. SUPPLEMENTARY INFORMATION: In FR Doc. FDA–2011–19331, appearing on page 45820 in the Federal Register of Monday, August 1, 2011, the following corrections are made: SUMMARY: PO 00000 Frm 00082 Fmt 4703 Sfmt 4703 [FR Doc. 2011–21895 Filed 8–25–11; 8:45 am] BILLING CODE 4160–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration Agency Information Collection Activities: Proposed Collection: Comment Request In compliance with the requirement for opportunity for public comment on proposed data collection projects (section 3506(c)(2)(A) of Title 44, United States Code, as amended by the Paperwork Reduction Act of 1995, Pub. L. 104–13), the Health Resources and Services Administration (HRSA) publishes periodic summaries of proposed projects being developed for submission to the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. To request more information on the proposed project or to obtain a copy of the data collection plans and draft instruments, e-mail paperwork@hrsa.gov or call the HRSA Reports Clearance Officer at (301) 443– 1129. Comments are invited on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the Agency; (b) the accuracy of the Agency’s estimate of the burden of the proposed collection of information; (c) ways to enhance the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Proposed Project: National Health Service Corps Site Survey (OMB No. 0915–0232)—Revision The Health Resources and Services Administration (HRSA), Bureau of Clinician Recruitment and Service (BCRS) places National Health Service Corps (NHSC) health care professionals at sites that provide services to underserved and vulnerable populations. The NHSC Site Survey E:\FR\FM\26AUN1.SGM 26AUN1

Agencies

[Federal Register Volume 76, Number 166 (Friday, August 26, 2011)]
[Notices]
[Page 53478]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-21895]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2011-N-0528]


Food Safety Modernization Act Domestic and Foreign Facility 
Reinspections, Recall, and Importer Reinspection User Fee Rates for 
Fiscal Year 2012; Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice; correction.

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SUMMARY: The Food and Drug Administration (FDA) is correcting a notice 
that appeared in the Federal Register of August 1, 2011 (76 FR 45820). 
The document announced the fiscal year 2012 fee rates for certain 
domestic and foreign facility reinspections, failure to comply with a 
recall order, and importer reinspections that are mandated in the FDA 
Food Safety Modernization Act (FSMA). The document was published with 
two typographical errors. This document corrects those errors.

FOR FURTHER INFORMATION CONTACT: Amy Waltrip, 12420 Parklawn Dr., Rm. 
2012, Rockville, MD 20857, 301-796-8811, e-mail: 
Amy.Waltrip@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: In FR Doc. FDA-2011-19331, appearing on page 
45820 in the Federal Register of Monday, August 1, 2011, the following 
corrections are made:
    1. On page 45822, in the second column, in the first line, ``$335'' 
is corrected to read ``$325''.
    2. On page 45822, in the second column, in ``Table 3--FSMA Fee 
Schedule for FY 2012,'' ``$335'' is corrected to read ``$325''.

    Dated: August 19, 2011.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2011-21895 Filed 8-25-11; 8:45 am]
BILLING CODE 4160-01-P

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