Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Recordkeeping Requirements for Microbiological Testing and Corrective Measures for Bottled Water, 39734 [2013-15793]

Download as PDF 39734 Federal Register / Vol. 78, No. 127 / Tuesday, July 2, 2013 / Notices TABLE 3—ESTIMATED ANNUAL THIRD-PARTY DISCLOSURES 1—Continued Number of respondents Activity/21 CFR section Total .......................................................... Number of disclosures per respondent Total annual disclosures Average burden per disclosure Total hours 2 ........................ ........................ ........................ ........................ 3,691,842 Total operating & maintenance costs 24,259,921 1 There are no capital costs associated with this collection of information. 2 Total hours have been rounded. 3 Refers to the facility component of the burden for this requirement. 4 Refers to the AB component of the burden for this requirement. 5 Refers to the situation where a patient specifically does not want to receive the lay summary of her exam. Dated: June 25, 2013. Leslie Kux, Assistant Commissioner for Policy. Dated: June 26, 2013. Leslie Kux, Assistant Commissioner for Policy. [FR Doc. 2013–15790 Filed 7–1–13; 8:45 am] [FR Doc. 2013–15795 Filed 7–1–13; 8:45 am] BILLING CODE 4160–01–P BILLING CODE 4160–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Food and Drug Administration [Docket No. FDA–2013–N–0033] [Docket No. FDA–2012–N–1108] Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Interstate Shellfish Dealer’s Certificate AGENCY: Food and Drug Administration, HHS. ACTION: AGENCY: Notice. The Food and Drug Administration (FDA) is announcing that a collection of information entitled ‘‘Interstate Shellfish Dealer’s Certificate’’ has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. FOR FURTHER INFORMATION CONTACT: Domini Bean, Office of Information Management, Food and Drug Administration, 1350 Piccard Dr., PI50– 400B, Rockville, MD 20850, 301–796– 5733, domini.bean@fda.hhs.gov. SUPPLEMENTARY INFORMATION: On March 25, 2013, the Agency submitted a proposed collection of information entitled, ‘‘Interstate Shellfish Dealer’s Certificate’’ to OMB for review and clearance under 44 U.S.C. 3507. An Agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. OMB has now approved the information collection and has assigned OMB control number 0910–0021. The approval expires on May 31, 2016. A copy of the supporting statement for this information collection is available on the Internet at https://www.reginfo.gov/ public/do/PRAMain. VerDate Mar<15>2010 17:51 Jul 01, 2013 Food and Drug Administration, HHS. SUMMARY: tkelley on DSK3SPTVN1PROD with NOTICES Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Recordkeeping Requirements for Microbiological Testing and Corrective Measures for Bottled Water Jkt 229001 ACTION: Notice. The Food and Drug Administration (FDA) is announcing that a collection of information entitled ‘‘Recordkeeping Requirements for Microbiological Testing and Corrective Measures for Bottled Water’’ has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. FOR FURTHER INFORMATION CONTACT: Domini Bean, Office of Information Management, Food and Drug Administration, 1350 Piccard Dr., PI50– 400B, Rockville, MD 20850, 301–796– 5733, domini.bean@fda.hhs.gov. SUPPLEMENTARY INFORMATION: On March 26, 2013, the Agency submitted a proposed collection of information entitled ‘‘Recordkeeping Requirements for Microbiological Testing and Corrective Measures for Bottled Water’’ to OMB for review and clearance under 44 U.S.C. 3507. An Agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. OMB has now approved the information collection and has assigned OMB control number 0910–0658. The approval expires on May 31, 2016. A SUMMARY: PO 00000 Frm 00031 Fmt 4703 Sfmt 4703 copy of the supporting statement for this information collection is available on the Internet at https://www.reginfo.gov/ public/do/PRAMain. Dated: June 26, 2013. Leslie Kux, Assistant Commissioner for Policy. [FR Doc. 2013–15793 Filed 7–1–13; 8:45 am] BILLING CODE 4160–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2013–N–0716] Agency Information Collection Activities; Proposed Collection; Comment Request; Designated New Animal Drugs for Minor Use and Minor Species AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (the PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the paperwork associated with designation under the Minor Use and Minor Species (MUMS) Act. DATES: Submit either electronic or written comments on the collection of information by September 3, 2013. ADDRESSES: Submit electronic comments on the collection of information to https:// www.regulations.gov. Submit written comments on the collection of information to the Division of Dockets Management (HFA–305), Food and Drug SUMMARY: E:\FR\FM\02JYN1.SGM 02JYN1

Agencies

[Federal Register Volume 78, Number 127 (Tuesday, July 2, 2013)]
[Notices]
[Page 39734]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-15793]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2013-N-0033]

Agency Information Collection Activities; Announcement of Office
of Management and Budget Approval; Recordkeeping Requirements for
Microbiological Testing and Corrective Measures for Bottled Water

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is announcing that a
collection of information entitled ``Recordkeeping Requirements for
Microbiological Testing and Corrective Measures for Bottled Water'' has
been approved by the Office of Management and Budget (OMB) under the
Paperwork Reduction Act of 1995.

FOR FURTHER INFORMATION CONTACT: Domini Bean, Office of Information
Management, Food and Drug Administration, 1350 Piccard Dr., PI50-400B,
Rockville, MD 20850, 301-796-5733, domini.bean@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: On March 26, 2013, the Agency submitted a
proposed collection of information entitled ``Recordkeeping
Requirements for Microbiological Testing and Corrective Measures for
Bottled Water'' to OMB for review and clearance under 44 U.S.C. 3507.
An Agency may not conduct or sponsor, and a person is not required to
respond to, a collection of information unless it displays a currently
valid OMB control number. OMB has now approved the information
collection and has assigned OMB control number 0910-0658. The approval
expires on May 31, 2016. A copy of the supporting statement for this
information collection is available on the Internet at https://www.reginfo.gov/public/do/PRAMain.

Dated: June 26, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013-15793 Filed 7-1-13; 8:45 am]
BILLING CODE 4160-01-P

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