60 day FRN

Federal Register / Vol. 82, No. 103 / Wednesday, May 31, 2017 / Notices
information contained in the notice
pursuant to exemption 4 of the Freedom
of Information Act (5 U.S.C. 552(b)(4)).
Board of Governors of the Federal Reserve
System, May 24, 2017.
Ann E. Misback,
Secretary of the Board.
[FR Doc. 2017–11136 Filed 5–30–17; 8:45 am]

Centers for Disease Control and
Prevention, Department of Health and
Human Services (HHS).
ACTION: Notice with comment period.

Change in Bank Control Notices;
Acquisitions of Shares of a Bank or
Bank Holding Company

nlaroche on DSK30NT082PROD with NOTICES

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 a proposed revision of the
information collection project titled
‘‘Health Hazard Evaluation and
Technical Assistance—Requests and
Emerging Problems.’’ This data
collection supports legislatively
mandated (PL 91–596) assistance
investigating emerging occupational
hazards in workplaces.
DATES: Written comments must be
received on or before July 31, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0050 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.
SUMMARY:

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 June 19,
2017.
A. Federal Reserve Bank of
Minneapolis (Jacquelyn K. Brunmeier,
Assistant Vice President) 90 Hennepin
Avenue, Minneapolis, Minnesota
55480–0291:
1. Mark Edward Davis, Saint Peter,
Minnesota, Stanley M. Davis Revocable
Trust, Stanley Martin Davis, Trustee,
Plymouth, Minnesota, Martin Edward
Davis, Excelsior, Minnesota, Mark
Mitchell, Davis, Excelsior, Minnesota; as
a group acting in concert; to acquire the
voting shares of Bancommunity Services
Corporation, Saint Peter, Minnesota,
and thereby indirectly acquire voting
shares of First National Bank Minnesota,
Saint Peter, Minnesota
Board of Governors of the Federal Reserve
System, May 25, 2017.
Yao-Chin Chao,
Assistant Secretary of the Board.

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 Leroy A.

FOR FURTHER INFORMATION CONTACT:

BILLING CODE 6210–01–P

14:54 May 30, 2017

[60 Day–17–0260; Docket No. CDC–2017–
0050]

AGENCY:

FEDERAL RESERVE SYSTEM

VerDate Sep<11>2014

Centers for Disease Control and
Prevention

Proposed Data Collections Submitted
for Public Comment and
Recommendations

BILLING CODE 6210–01–P

[FR Doc. 2017–11209 Filed 5–30–17; 8:45 am]

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

Jkt 241001

PO 00000

Frm 00038

Fmt 4703

Sfmt 4703

24971

Richardson, Information Collection
Review Office, Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., MS–D74, Atlanta, Georgia
30329; phone: 404–639–7570; Email:
[email protected].
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
Health Hazard Evaluation and
Technical Assistance—Requests and
Emerging Problems (OMB Control No.

E:\FR\FM\31MYN1.SGM

31MYN1

24972

Federal Register / Vol. 82, No. 103 / Wednesday, May 31, 2017 / Notices

0920–0260, Expiration 11/30/2017)—
Revision—National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
In accordance with its mandates
under the Occupational Safety and
Health Act of 1970 and the Federal
Mine Safety and Health Act of 1977, the
National Institute for Occupational
Safety and Health (NIOSH) responds to
requests for health hazard evaluations
(HHE) to identify chemical, biological or
physical hazards in workplaces
throughout the United States. Each year,
NIOSH receives approximately 290 such
requests. Most HHE requests come from
the following types of companies:
service, manufacturing, health and
social services, transportation,
agriculture, mining, skilled trade and
construction. NIOSH is requesting a
three year approval time.
A printed Health Hazard Evaluation
request form is available in English and
in Spanish. The form is also available
on the Internet and differs from the
printed version only in format and in
the fact that it can be submitted directly
from the Web site. The request form
takes an estimated 12 minutes to
complete. The form provides the
mechanism for employees, employers,
and other authorized representatives to
supply the information required by the
regulations governing the NIOSH Health
Hazard Evaluation program (42 CFR
85.3–1). If employees are submitting the
form it must contain the signatures of
three or more current employees.
However, regulations allow a single
signature if the requestor: is one of three
(3) or fewer employees in the process,
operation, or job of concern; or is any
officer of a labor union representing the
employees for collective bargaining
purposes. An individual management
official may request an evaluation on
behalf of the employer. The information
provided is used by NIOSH to
determine whether there is reasonable
cause to justify conducting an
investigation and provides a mechanism
to respond to the requestor.

NIOSH reviews the HHE request to
determine if an on-site evaluation is
needed. The primary purpose of an onsite evaluation is to help employers and
employees identify and eliminate
occupational health hazards. For 40% of
the requests received NIOSH determines
an on-site evaluation is needed. When
an on-site evaluation is not done,
NIOSH prepares and provides a written
report after gathering information from
the requester(s) and reviewing available
exposure and health records.
In about 70% of on-site evaluations
(presently estimated to be 122 facilities
a year) employees are interviewed
individually to learn about health
problems and possible contributing
factors at work. Interviews may take
approximately 15 minutes per
respondent. The interview questions are
specific to each workplace and its
suspected diseases and hazards.
However, interviews are based on
standard medical practices.
In approximately 30% of on-site
evaluations that involve employee
interviews (presently estimated to be 37
out of 122 facilities a year),
questionnaires are distributed to the
employees (averaging about 100
employees per site). Questionnaires may
require approximately 30 minutes to
complete. The survey questions are
specific to each workplace and its
suspected diseases and hazards,
however, items in the questionnaires are
derived from standardized or widely
used medical and epidemiologic data
collection instruments.
About 70% of the on-site evaluations
involve employee exposure monitoring
in the workplace. Employees who agree
to participate wear a sampler or
monitoring device to measure personal
workplace exposures. They are offered
the opportunity to get a written notice
of their exposure results. To indicate
their preference, employees complete a
contact card. Completing a contact card
may take 5 minutes or less. The number
of employees monitored for workplace
exposures per on-site evaluation may
vary from none up to about 25. In some
instances, however, the number can be
much greater.

NIOSH distributes interim and final
reports of health hazard evaluations,
excluding personal identifiers, to:
Requesters, employers, employee
representatives; the Department of Labor
(Occupational Safety and Health
Administration or Mine Safety and
Health Administration, as appropriate);
state health departments; and, as
needed, other state and federal agencies.
NIOSH administers a follow-back
program to assess the effectiveness of its
HHE program in reducing workplace
hazards. NIOSH distributes follow-back
questionnaires to the primary employer
and employee representative at all the
workplaces where NIOSH conducted an
on-site evaluation. In a small number of
instances, a follow-back on-site
evaluation may be completed. The first
follow-back questionnaire is distributed
shortly after the first visit for an on-site
evaluation and takes about 10 minutes
to complete. A second follow-back
questionnaire is distributed a month
after the final report and requires about
20 minutes to complete. At 24 months,
a third follow-back questionnaire is
distributed which takes about 15
minutes to complete.
For requests where NIOSH does not
conduct an on-site evaluation, the
requestor receives the first follow-back
questionnaire 1 month after our report
and a second one 12 months after our
response. The first questionnaire takes
about 10 minutes to complete and the
second questionnaire takes about 15
minutes to complete.
Because of the number of
investigations conducted each year, the
need to respond quickly to requests for
assistance, the diverse and
unpredictable nature of these
investigations, and its follow-back
program to assess evaluation
effectiveness; NIOSH requests a
consolidated clearance for data
collections performed within the
domain of its HHE program. There is no
cost to respondents other than their
time. The total estimated annual burden
hours is 2,960.

nlaroche on DSK30NT082PROD with NOTICES

ESTIMATE OF ANNUALIZED BURDEN HOURS
Number of
respondents

Type of respondent

Form

Employees and Representatives .....

Health Hazard Evaluation Request
Form.
Health Hazard Evaluation Request
Form.
Health Hazard Evaluation specific
interview example.

Employers ........................................
Employees .......................................

VerDate Sep<11>2014

14:54 May 30, 2017

Jkt 241001

PO 00000

Frm 00039

Fmt 4703

Sfmt 4703

Number of
responses per
respondent

Average
burden per
response
in hours

Total burden
hours

203

1

12/60

41

87

1

12/60

18

2,580

1

15/60

645

E:\FR\FM\31MYN1.SGM

31MYN1

24973

Federal Register / Vol. 82, No. 103 / Wednesday, May 31, 2017 / Notices
ESTIMATE OF ANNUALIZED BURDEN HOURS—Continued
Average
burden per
response
in hours

Number of
responses per
respondent

Total burden
hours

Form

Employees .......................................

Health Hazard Evaluation specific
questionnaire example.
Contact information post card .........
First followback questionnaire .........
Second followback questionnaire ....

3,700

1

30/60

1,850

2,150
244
244

1
1
1

5/60
10/60
20/60

180
41
82

Third followback questionnaire ........

244

1

15/60

61

First followback questionnaire .........

98

1

10/60

17

Second followback questionnaire ....

98

1

15/60

25

..........................................................

........................

..........................

........................

2,960

Employees .......................................
Employees and Representatives;
Employers—Year 1 (on-site evaluation).
Employees and Representatives;
Employers—Year 2 (on-site evaluation).
Employees and Representatives;
Employers—Year 1 (without onsite evaluation).
Employees and Representatives;
Employers—Year 2 (without onsite evaluation).
Total ..........................................

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. 2017–11111 Filed 5–30–17; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–1036; Docket No. CDC–2017–
0051]

Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention, 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 ‘‘Community Assessment
for Public Health Emergency Response
(CASPER).’’ CASPER is an effective
public health tool designed to quickly
provide low-cost, household-based
information about a community’s needs
and health status in a simple, easy-tounderstand format for decision makers.

SUMMARY:

nlaroche on DSK30NT082PROD with NOTICES

Number of
respondents

Type of respondent

VerDate Sep<11>2014

14:54 May 30, 2017

Jkt 241001

Written comments must be
received on or before July 31, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0051 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 Leroy A.
Richardson, Information Collection
Review Office, Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., MS–D74, Atlanta, Georgia
30329; phone: 404–639–7570; Email:
[email protected].
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
DATES:

PO 00000

Frm 00040

Fmt 4703

Sfmt 4703

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

E:\FR\FM\31MYN1.SGM

31MYN1