Proposed Data Collection Submitted for Public Comment and Recommendations, 40698-40700 [2016-14726]
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40698
Federal Register / Vol. 81, No. 120 / Wednesday, June 22, 2016 / Notices
Title: Hanjin/Zim Slot Exchange
Agreement.
Parties: Hanjin Shipping Co., Ltd. and
Zim Integrated Shipping Services, Ltd.
Filing Party: Mark E. Newcomb; ZIM
American Integrated Shipping Services
Co., LLC; 5801 Lake Wright Dr., Norfolk,
VA 23508.
Synopsis: The amendment would add
Taiwan, Malaysia, and Singapore to the
geographic scope, and increase the slot
sale and purchase authority to 2,000
TEUs per sailing.
Agreement No.: 012293–006.
Title: Maersk/MSC Vessel Sharing
Agreement.
Parties: Maersk Line A/S and MSC
Mediterranean Shipping Company S.A.
Filing Party: Wayne Rohde, Esq.;
Cozen O’Connor; 1200 Nineteenth St.
NW., Washington, DC 20036.
Synopsis: The Amendment would
increase the number of vessels the
Parties are authorized to operate in the
U.S. trades.
By Order of the Federal Maritime
Commission.
Dated: June 17, 2016.
Rachel E. Dickon,
Assistant Secretary.
[FR Doc. 2016–14814 Filed 6–21–16; 8:45 am]
Board of Governors of the Federal Reserve
System, June 17, 2016.
Michele T. Fennell,
Assistant Secretary of the Board.
BILLING CODE 6731–AA–P
FEDERAL RESERVE SYSTEM
[FR Doc. 2016–14737 Filed 6–21–16; 8:45 am]
BILLING CODE 6210–01–P
mstockstill on DSK3G9T082PROD with NOTICES
Change in Bank Control Notices;
Acquisitions of Shares of a Bank or
Bank Holding Company
FEDERAL RESERVE SYSTEM
The notificants listed below have
applied under the Change in Bank
Control Act (12 U.S.C. 1817(j)) and
§ 225.41 of the Board’s Regulation Y (12
CFR 225.41) to acquire shares of a bank
or bank holding company. The factors
that are considered in acting on the
notices are set forth in paragraph 7 of
the Act (12 U.S.C. 1817(j)(7)).
The notices are available for
immediate inspection at the Federal
Reserve Bank indicated. The notices
also will be available for inspection at
the offices of the Board of Governors.
Interested persons may express their
views in writing to the Reserve Bank
indicated for that notice or to the offices
of the Board of Governors. Comments
must be received not later than July 7,
2016.
A. Federal Reserve Bank of Cleveland
(Nadine Wallman, Vice President) 1455
East Sixth Street, Cleveland, Ohio
44101–2566. Comments can also be sent
electronically to
Comments.applications@clev.frb.org:
1. Helen Parrish Beach, Lexington,
Kentucky, to acquire voting shares as
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20:02 Jun 21, 2016
Jkt 238001
part of a family control group of
Genbeach Company, Inc., Winchester,
Kentucky and thereby indirectly retain
control of Peoples Exchange Bank,
Winchester, Kentucky.
B. Federal Reserve Bank of
Philadelphia (William Spaniel, Senior
Vice President) 100 North 6th Street,
Philadelphia, Pennsylvania 19105–
1521. Comments can also be sent
electronically to
Comments.applications@phil.frb.org:
1. The Willits Family Partnership, and
its proposed general partner, the Lydia
Willits Bartholomew Trust #2, each of
Malvern, Pennsylvania, and its trustee
Jamie Bartholomew Aller, West Chester,
Pennsylvania, together with the Lydia
Willits Bartholomew Trust #1, Malvern,
Pennsylvania, Andrew Marshall
Bartholomew II, Malvern, Pennsylvania,
and William Brinton Bartholomew,
William Evans Lincoln Howard V, and
Lydia Willits Bartholomew, each of West
Chester, Pennsylvania, all together a
group acting in concert to acquire voting
shares of Malvern Bank Corporation,
Malvern, Pennsylvania and thereby
indirectly acquire shares of The
National Bank of Malvern, Malvern,
Pennsylvania.
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
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Sfmt 4703
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than July 18, 2016.
A. Federal Reserve Bank of Kansas
City (Dennis Denney, Assistant Vice
President) 1 Memorial Drive, Kansas
City, Missouri 64198–0001:
1. Citizens National Corporation,
Wisner, Nebraska; to acquire up to an
additional 0.57 percent, for a total of
35.12 percent of the voting shares of
Republic Corporation, and thereby
indirectly acquire control of United
Republic Bank, both of Omaha,
Nebraska.
Board of Governors of the Federal Reserve
System, June 17, 2016.
Michele Taylor Fennell,
Assistant Secretary of the Board.
[FR Doc. 2016–14749 Filed 6–21–16; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–16ARH; Docket No. CDC–2016–
0053]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on the proposed information
collection entitled ‘‘Poison Center
Collaborations for Public Health
Emergencies.’’ The goal for this new
information collection is to create a
timely generic clearance mechanism to
allow a network of U.S. poison centers,
in collaboration with CDC, to obtain
SUMMARY:
E:\FR\FM\22JNN1.SGM
22JNN1
Federal Register / Vol. 81, No. 120 / Wednesday, June 22, 2016 / Notices
critical exposure and health information
during public health emergencies. CDC
will collect follow-up information not
captured during poison center callers’
initial calls.
DATES: Written comments must be
received on or before August 22, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0053 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.
To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
mstockstill on DSK3G9T082PROD with NOTICES
FOR FURTHER INFORMATION CONTACT:
VerDate Sep<11>2014
20:02 Jun 21, 2016
Jkt 238001
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (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; (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; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Poison Center Collaborations for
Public Health Emergencies—NEW—
National Center for Environmental
Health (NCEH), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Centers for Disease Control and
Prevention (CDC) is requesting a threeyear Paperwork Reduction Act (PRA)
clearance for a new generic clearance
information collection request (Generic
ICR) titled ‘‘Poison Center
Collaborations for Public Health
Emergencies.’’
CDC’s key partner, the American
Association of Poison Control Centers
(AAPCC), is a national network of 55
poison centers working to prevent and
treat poison exposures. The goal for this
new Generic ICR is to create a timely
mechanism to allow poison centers, in
collaboration with CDC, to obtain
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Sfmt 4703
40699
critical exposure and health information
during public health emergencies. This
information is not captured during
initial poison center calls about triage
and treatment of potential poison
exposures. Additional data collections
are needed quickly to further
characterize exposures, risk factors, and
illnesses.
When a public health emergency of
interest to CDC and AAPCC occurs, the
CDC and AAPCC hold a meeting to
mutually decide whether the incident
needs further investigation. For a public
health emergency to be selected for callback, adverse health effects must have
occurred and a response is needed to
prevent further morbidity and mortality.
The event must meet the criteria below:
(1) The event is a public health
emergency causing adverse health
effects.
(2) Timely data are urgently needed to
inform rapid public health action to
prevent or reduce injury, disease, or
death.
(3) The event is characterized by a
natural or man-made disaster,
contaminated food or water, a new or
existing consumer product, or an
emerging public health threat.
(4) The event has resulted in calls to
a poison center, and the poison center
agrees to conduct the call-back data
collection.
(5) The event is domestic.
(6) Data collection will be completed
in 60 days or less.
Trained poison center staff will
conduct the call-back telephone survey,
after administering consent.
Respondents will include individuals
who call poison centers about exposures
related to the select public health
emergencies. These respondents include
adults, 18 years and older; adolescents,
15 to less than 18 years; and parents or
guardians on behalf of their children
less than 15 years of age.
The total estimate of 300 annual
respondents is based on poison center
experience which assumes two
incidents per year with approximately
150 respondents per event. The average
burden per respondent is approximately
40 minutes for the call-back
questionnaire. We anticipate a total
annualized burden of 200 hours.
There is no cost to the respondents
other than their time.
E:\FR\FM\22JNN1.SGM
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40700
Federal Register / Vol. 81, No. 120 / Wednesday, June 22, 2016 / Notices
ESTIMATED ANNUAL REPORTING BURDEN
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
(in hours)
Total burden
hours
Type of respondent
Form name
Adult Poison Center Callers .............
Adolescent Poison Center Callers ....
Parent or Guardian Poison Center
Callers.
Call-back Questionnaire for Self ......
Call-back Questionnaire for Self ......
Call-back Questionnaire for Proxy ...
210
30
60
1
1
1
40/60
40/60
40/60
140
20
40
Total ...........................................
...........................................................
........................
........................
........................
200
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2016–14726 Filed 6–21–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Please note: All public comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.
Centers for Disease Control and
Prevention
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on Using the Standardized
National Hypothesis Generating
Questionnaire during Multistate
Investigations of Foodborne Disease
Clusters and Outbreaks.
DATES: Written comments must be
received on or before August 22, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0054 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
mstockstill on DSK3G9T082PROD with NOTICES
VerDate Sep<11>2014
20:02 Jun 21, 2016
Jkt 238001
To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (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
FOR FURTHER INFORMATION CONTACT:
[60Day–16–0997; Docket No. CDC–2016–
0054]
SUMMARY:
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
PO 00000
Frm 00048
Fmt 4703
Sfmt 4703
clarity of the information to be
collected; (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; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Standardized National Hypothesis
Generating Questionnaire (0920–0997,
Expiration Date 10/31/2016)—
Revision—National Center for Emerging
and Zoonotic Infectious Diseases
(NCEZID), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
It is estimated that each year roughly
1 in 6 Americans gets sick, 128,000 are
hospitalized, and 3,000 die of foodborne
diseases. CDC and partners ensure rapid
and coordinated surveillance, detection,
and response to multistate outbreaks, to
limit the number of illnesses, and to
learn how to prevent similar outbreaks
from happening in the future.
Conducting interviews during the
initial hypothesis-generating phase of
multistate foodborne disease outbreaks
presents numerous challenges. In the
U.S. there is not a standard, national
form or data collection system for
illnesses caused by many enteric
E:\FR\FM\22JNN1.SGM
22JNN1
]]>Agencies
[Federal Register Volume 81, Number 120 (Wednesday, June 22, 2016)]
[Notices]
[Pages 40698-40700]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-14726]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-16-16ARH; Docket No. CDC-2016-0053]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing efforts to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies to take this opportunity to comment on proposed and/or
continuing information collections, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on the proposed
information collection entitled ``Poison Center Collaborations for
Public Health Emergencies.'' The goal for this new information
collection is to create a timely generic clearance mechanism to allow a
network of U.S. poison centers, in collaboration with CDC, to obtain
[[Page 40699]]
critical exposure and health information during public health
emergencies. CDC will collect follow-up information not captured during
poison center callers' initial calls.
DATES: Written comments must be received on or before August 22, 2016.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2016-
0053 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Leroy A. Richardson, Information Collection Review
Office, Centers for Disease Control and Prevention 1600 Clifton Road
NE., MS-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. All relevant comments received will be posted
without change to Regulations.gov, including any personal information
provided. For access to the docket to read background documents or
comments received, go to Regulations.gov.
Please note: All public comment should be submitted through the
Federal eRulemaking portal (Regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact the Information Collection Review Office,
Centers for Disease Control and Prevention, 1600 Clifton Road NE., MS-
D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. In addition, the PRA also requires
Federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
Comments are invited on: (a) Whether the proposed collection of
information is necessary for the proper performance of the functions of
the agency, including whether the information shall have practical
utility; (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; (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; and (e) estimates of capital or start-
up costs and costs of operation, maintenance, and purchase of services
to provide information. Burden means the total time, effort, or
financial resources expended by persons to generate, maintain, retain,
disclose or provide information to or for a Federal agency. This
includes the time needed to review instructions; to develop, acquire,
install and utilize technology and systems for the purpose of
collecting, validating and verifying information, processing and
maintaining information, and disclosing and providing information; to
train personnel and to be able to respond to a collection of
information, to search data sources, to complete and review the
collection of information; and to transmit or otherwise disclose the
information.
Proposed Project
Poison Center Collaborations for Public Health Emergencies--NEW--
National Center for Environmental Health (NCEH), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Centers for Disease Control and Prevention (CDC) is requesting a
three-year Paperwork Reduction Act (PRA) clearance for a new generic
clearance information collection request (Generic ICR) titled ``Poison
Center Collaborations for Public Health Emergencies.''
CDC's key partner, the American Association of Poison Control
Centers (AAPCC), is a national network of 55 poison centers working to
prevent and treat poison exposures. The goal for this new Generic ICR
is to create a timely mechanism to allow poison centers, in
collaboration with CDC, to obtain critical exposure and health
information during public health emergencies. This information is not
captured during initial poison center calls about triage and treatment
of potential poison exposures. Additional data collections are needed
quickly to further characterize exposures, risk factors, and illnesses.
When a public health emergency of interest to CDC and AAPCC occurs,
the CDC and AAPCC hold a meeting to mutually decide whether the
incident needs further investigation. For a public health emergency to
be selected for call-back, adverse health effects must have occurred
and a response is needed to prevent further morbidity and mortality.
The event must meet the criteria below:
(1) The event is a public health emergency causing adverse health
effects.
(2) Timely data are urgently needed to inform rapid public health
action to prevent or reduce injury, disease, or death.
(3) The event is characterized by a natural or man-made disaster,
contaminated food or water, a new or existing consumer product, or an
emerging public health threat.
(4) The event has resulted in calls to a poison center, and the
poison center agrees to conduct the call-back data collection.
(5) The event is domestic.
(6) Data collection will be completed in 60 days or less.
Trained poison center staff will conduct the call-back telephone
survey, after administering consent. Respondents will include
individuals who call poison centers about exposures related to the
select public health emergencies. These respondents include adults, 18
years and older; adolescents, 15 to less than 18 years; and parents or
guardians on behalf of their children less than 15 years of age.
The total estimate of 300 annual respondents is based on poison
center experience which assumes two incidents per year with
approximately 150 respondents per event. The average burden per
respondent is approximately 40 minutes for the call-back questionnaire.
We anticipate a total annualized burden of 200 hours.
There is no cost to the respondents other than their time.
[[Page 40700]]
Estimated Annual Reporting Burden
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response Total burden
respondents respondent (in hours) hours
----------------------------------------------------------------------------------------------------------------
Adult Poison Center Callers... Call-back 210 1 40/60 140
Questionnaire
for Self.
Adolescent Poison Center Call-back 30 1 40/60 20
Callers. Questionnaire
for Self.
Parent or Guardian Poison Call-back 60 1 40/60 40
Center Callers. Questionnaire
for Proxy.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 200
----------------------------------------------------------------------------------------------------------------
Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2016-14726 Filed 6-21-16; 8:45 am]
BILLING CODE 4163-18-P
