June 13, 2012 – Federal Register Recent Federal Regulation Documents

Reader Aids
Document Number: FR-2012-06-13-ReaderAids
Type: Reader Aids
Date: 2012-06-13
National Science Board; Sunshine Act Meetings
Document Number: 2012-14560
Type: Notice
Date: 2012-06-13
Agency: National Science Foundation, Agencies and Commissions
National Science Board; Sunshine Act Meetings
Document Number: 2012-14558
Type: Notice
Date: 2012-06-13
Agency: National Science Foundation, Agencies and Commissions
Improving Repayment Options for Federal Student Loan Borrowers
Document Number: 2012-14537
Type: Administrative Order
Date: 2012-06-13
Agency: Executive Office of the President
Privacy and Security of Information Stored on Mobile Communications Devices
Document Number: 2012-14496
Type: Proposed Rule
Date: 2012-06-13
Agency: Federal Communications Commission, Agencies and Commissions
This document seeks comment on the privacy and data security practices of mobile wireless services providers with respect to customer information stored on their users' mobile communications devices. In addition, the document seeks comment on the application of existing privacy and security requirements to such information.
Renewal of Approved Information Collection
Document Number: 2012-14494
Type: Notice
Date: 2012-06-13
Agency: Department of the Interior, Bureau of Land Management
In compliance with the Paperwork Reduction Act, the Bureau of Land Management (BLM) invites public comments on, and plans to request approval to continue, the collection of information from applicants for a land patent under the Color-of-Title Act. The Office of Management and Budget (OMB) has assigned control number 1004-0029 to this information collection.
Sunshine Act Meeting
Document Number: 2012-14491
Type: Notice
Date: 2012-06-13
Agency: International Trade Commission, Agencies and Commissions
Sunshine Act Meeting
Document Number: 2012-14490
Type: Notice
Date: 2012-06-13
Agency: International Trade Commission, Agencies and Commissions
Center for Scientific Review; Notice of Meeting
Document Number: 2012-14481
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review; Notice of Closed Meetings
Document Number: 2012-14480
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
National Institute of General Medical Sciences; Notice of Closed Meeting
Document Number: 2012-14478
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review; Notice of Closed Meetings
Document Number: 2012-14474
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
User Fee Schedule for Trade Promotion Services
Document Number: 2012-14472
Type: Notice
Date: 2012-06-13
Agency: Department of Commerce, International Trade Administration
The U.S. & Foreign Commercial Service (US&FCS) within the International Trade Administration (ITA) publishes this notice to announce its intent to adjust user fees in light of an independent cost of service study finding, which concluded that the US&FCS is not fully covering its costs for providing trade promotion services under the current fee structure. ITA provides a wide range of trade promotion information and services to U.S. businesses that are exporting or seeking to export. The services considered here are a subset of ITA activities that involve relatively more intensive time engagements with particular client firms; ITA will continue to provide its core information and services without charge. The primary objective of the adjustment to the User Fee Schedule is to ensure that the fees for the more intensive services reflect, to the extent possible, the actual costs incurred by the United States for providing these more intensive trade promotion services. The fee revenue is expected to continue to contribute to ITA's capabilities for assisting U.S. businesses in accessing export markets. In addition, in revising the user fees, the US&FCS proposes to revise the small & medium-sized enterprises (SME) hourly rate discount as well as the SME incentive program piloted in 2008. The US&FCS has historically offered a discount to SME's, defined as those which employ 500 or less persons. Under the User Fee Schedule proposed in this notice, US&FCS will offer a discount of 50 percent per hour to SMEs. The purpose of this notice is to align user fees and authorized activities with actual program costs; and improve our ability to properly recover direct and indirect costs associated with service delivery.
Agency Information Collection Activities: Form I-601, Revision of a Currently Approved Information Collection; Correction
Document Number: 2012-14470
Type: Notice
Date: 2012-06-13
Agency: Department of Homeland Security, U.S. Citizenship and Immigration Services
Safety Zone; NOAA Vessel Rueben Lasker Launch, Marinette, WI
Document Number: 2012-14468
Type: Rule
Date: 2012-06-13
Agency: Coast Guard, Department of Homeland Security
The Coast Guard is establishing a temporary safety zone on the Menominee River in Marinette, WI. This zone is intended to restrict vessels from a portion of Menominee River during the launching of the NOAA vessel, Rueben Lasker, on June 16, 2012. This temporary safety zone is necessary to protect the surrounding public and vessels from the hazards associated with the launching of this large vessel.
Advisory Committee on the Records of Congress; Meeting
Document Number: 2012-14466
Type: Notice
Date: 2012-06-13
Agency: National Archives and Records Administration, Agencies and Commissions
In accordance with the Federal Advisory Committee Act, the National Archives and Records Administration (NARA) announces a meeting of the Advisory Committee on the Records of Congress. The committee advises NARA on the full range of programs, policies, and plans for the Center for Legislative Archives in the Office of Legislative Archives, Presidential Libraries, and Museum Services (LPM). The meeting is open to the public.
Fogarty International Center 2013 Strategic Plan
Document Number: 2012-14465
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
The Fogarty International Center (FIC), National Institutes of Health (NIH) is updating its strategic plan. To anticipate and set priorities for global health research and research training, FIC requests input from scientists, the general public, and interested parties. The goal of this strategic planning process is to identify current and future needs and directions for global health research and research training. The existing FIC strategic plan can be viewed at: https://www.fic.nih.gov/About/Pages/Strategic-Plan.aspx.
Proposed Collection; Comment Request: Process Evaluation of the Early Independence Award (EIA) Program
Document Number: 2012-14464
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for opportunity for public comment on proposed data collection projects, the Office of Strategic Coordination (OSC), Division of Program Coordination, Planning, and Strategic Initiatives (DPCPSI), National Institutes of Health (NIH), will publish periodic summaries of proposed projects to be submitted to the Office of Management and Budget (OMB) for review and approval. Proposed Collection: Title: Process Evaluation of the Early Independence Award (EIA) Program. Type of Information Collection Request: NEW. Need and Use of Information Collection: This study will assess the EIA program operations. The primary objectives of the study are to (1) assess if the requests for applications (RFAs) are meeting the needs of applicants, (2) document the selection process, (3) document EIA program operations, (4) assess the progress being made by the Early Independence Principal Investigators, and (5) assess the support provided by the Host Institutions to the Early Independence Principal Investigators. The findings will provide valuable information concerning (1) aspects of the program that could be revised or improved, (2) progress made by the Early Independence Principal Investigators, and (3) implementation of the program at Host Institutions. Frequency of Response: On occasion. Affected Public: None. Type of Respondents: Applicants, reviewers, and awardees. The annual reporting burden is as follows: Estimated Number of Respondents: 390; Estimated Number of Responses per Respondent: 1; Average Burden Hours per Response: 4; and Estimated Total Annual Burden Hours Requested: 158. The annualized cost to respondents is estimated at: $9,774. There are no Capital Costs to report. There are no Operating or Maintenance Costs to report.
National Cancer Institute; Notice of Meeting
Document Number: 2012-14463
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Proposed Collection; Comment Request: Opinions and Perspectives About the Current Blood Donation Policy for Men Who Have Sex With Men
Document Number: 2012-14462
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Under the provisions of Section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, the National Heart, Lung, and Blood Institute (NHLBI), the National Institutes of Health (NIH) has submitted to the Office of Management and Budget (OMB) a request for review and approval of the information collection listed below. This proposed information collection was previously published in the Federal Register in Volume 77 on February 23, 2012, page 10756, and allowed 60-days for public comment. Six written comments were received, one of which was shared by two signatories. One comment was a personal opinion regarding the current federal blood donation policy for men who have sex with men. Two of the written comments supported the study goals and design as proposed. Three of the written comments suggested changes to some of the questions, or asked whether the scope of the study could be expanded. As a result, content pertaining to the sexual histories of survey respondents was expanded to inform the broader context for the current policy for men who have sex with men. The purpose of this notice is to allow an additional 30 days for public comment. The National Institutes of Health may not conduct or sponsor, and the respondent is not required to respond to, an information collection that has been extended, revised, or implemented on or after October 1, 1995, unless it displays a currently valid OMB control number. Proposed Collection: Title: Opinions and Perspectives about the Current Blood Donation Policy for Men Who Have Sex with Men. Type of Information Collection Request: New. Need and Use of Information Collection: The current policy for blood donation in the U.S. with respect to men who have sex with men (MSM) is that any man who discloses having had sex with another man since 1977 is deferred indefinitely from donating. However, data from donors who have tested disease marker positive and were interviewed regarding potential risk factors suggest that some individuals continue to donate blood without disclosing MSM activity in contravention of the policy. In the 1980s there were surveillance studies of risk factors among donors who were determined to be HIV positive in pre-donation testing: Results indicated MSM behavior to be a risk factor for 56% of male donors. In addition, as part of the Retrovirus Epidemiology Donor Study (REDS), when anonymously surveyed by paper and pencil mailed surveys, 1.2% of male blood donors reported MSM behavior. In a 2007 study conducted in Sweden, 19% of 334 MSM who responded to a survey that was included in a monthly publication targeted to the Lesbian, Gay, Bisexual and Transgender (LGBT) community reported donating blood at least one-time since 1985. The authors suggested that MSM donors may be motivated by perceived discrimination, particularly younger MSM. Recent publications from the United Kingdom have reported what are likely the only population-based assessment of non-compliance with a similar restriction on blood donation for the MSM population as in the U.S.; this study was conducted in 2009 and 2010 and also estimated opinions about and self-reported intended compliance with the MSM deferral policy in place in the United Kingdom at that time. Note, the policy in the United Kingdom was modified in November 2011 and MSM in the United Kingdom are now allowed to donate if they have not been sexually active for a one-year period before donation. Data similar to those collected in Sweden and the United Kingdom are not available for the U.S. Potential changes to the current MSM policy for blood donation requires additional data, including information about motivating factors and compliance with the current MSM policy or a modified policy in the MSM population and in current blood donors. Speculative analyses have been conducted but do not directly address important considerations related to this policy such as the current level of compliance (in the MSM population) and non- compliance (in the blood donor population). While many scientists and ethicists have expressed opinions in support or against modification of the current MSM policy for blood donation, there is a lack of data that directly addresses important aspects of this policy debate. The proposed study will build off the studies conducted in Sweden and the United Kingdom and will collect directly relevant information on this topic by estimating the prevalence of compliance and non-compliance with the current MSM policy and assessing motivations for blood donation in the U.S. MSM population. Three research aims drive this study's protocols to provide valuable evidence on the motivations and compliance behaviors in the MSM and blood donor populations. The four geographic areas where the study will be conducted include the State of Connecticut, Western Pennsylvania, Southern Wisconsin, and the Bay Area of California. The first aim seeks to assess opinions about and common themes within the MSM population with respect to blood donation and the current MSM policy. Specifically, within a population of self- identified MSM in the U.S., what common themes can be identified regarding knowledge and opinions of current blood donation eligibility, and would opinions, including self-reported intended compliance, improve if the current MSM policy were changed to a deferral of a defined shorter duration? Another objective is to use what is learned in the focus groups to help select proper venues for identifying MSM who might be interested in participating in a comprehensive survey to assess compliance and non-compliance with the current MSM policy (see second aim). The second aim seeks to assess compliance and non-compliance in the MSM population with the current MSM blood donation policy by confidentially surveying two populations. One survey will be conducted in the MSM community to provide better estimates of compliance and non- compliance with the current policy and a second survey will be conducted in male blood donors to evaluate how frequently men who have had sex with another man since 1977 are donating blood. The surveys will be conducted using an instrument that includes common content to maximize the comparability of the responses. Both surveys will be conducted using Internet-based techniques and currently available software (SurveyGizmo, www.surveygizmo.com). The third aim seeks to assess motivations for donating in the group of self-identified MSM who are active blood donors in the U.S. Participants from the four geographic areas who report donating blood or the intention to donate will be asked to participate in confidential qualitative telephone interviews to identify their reasons for donating or wanting to donate blood. Frequency of Response: Once. Affected Public: Individuals. Type of Respondents: Males 18 years old or older. The annual reporting burden is as follows: Estimated Number of Respondents: 4864; Estimated Number of Responses per Respondent: 1 per respondent for 4844 respondents and 2 per respondent for 20 respondents; Average Burden of Hours per Response: 1.5 hours for Aim 1, 0.33 hour for Aim 2, and 1.0 hour for Aim 3; and Estimated Total Annual Burden Hours Requested: 1,700. The annualized total cost to all respondents is estimated at: $13,600 (based on $8.00 per hour). There are no Capital Costs to report. There are no Operating or Maintenance Costs to report.
National Institute of Mental Health; Notice of Closed Meeting
Document Number: 2012-14461
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Confidentiality of Information; Magnuson-Stevens Fishery Conservation and Management Reauthorization Act
Document Number: 2012-14460
Type: Proposed Rule
Date: 2012-06-13
Agency: Department of Commerce, National Oceanic and Atmospheric Administration
The National Marine Fisheries Service (NMFS) is extending the date by which public comments are due concerning proposed regulations to revise existing regulations governing the confidentiality of information submitted in compliance with any requirement or regulation under the Magnuson-Stevens Fishery Conservation and Management Act (Magnuson-Stevens Act or MSA). NMFS published the proposed rule on May 23, 2012 and announced that the public comment period would end on June 22, 2012. With this notice, NMFS is extending the comment period to August 21, 2012.
National Institute of Mental Health; Notice of Closed Meetings
Document Number: 2012-14459
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Atlantic Highly Migratory Species; Commercial Atlantic Region Non-Sandbar Large Coastal Shark Fishery Opening Date
Document Number: 2012-14458
Type: Notice
Date: 2012-06-13
Agency: Department of Commerce, National Oceanic and Atmospheric Administration
NMFS is announcing the opening date of the commercial Atlantic region non-sandbar large coastal shark fishery. This action is necessary to inform fishermen and dealers about the fishery opening date.
Advisory Committee for Aviation Consumer Protection
Document Number: 2012-14456
Type: Notice
Date: 2012-06-13
Agency: Department of Transportation, Office of the Secretary
This notice announces the first meeting of the Advisory Committee for Aviation Consumer Protection.
National Institute of Diabetes and Digestive and Kidney Diseases; Notice of Closed Meeting
Document Number: 2012-14453
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Biotech Life Sciences Trade Mission to Australia
Document Number: 2012-14452
Type: Notice
Date: 2012-06-13
Agency: Department of Commerce, International Trade Administration
National Institute on Drug Abuse-Notice of Closed Meetings
Document Number: 2012-14451
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Qualified Hydro 24, LLC; Notice of Cancellation of Scoping Meetings and Environmental Site Review
Document Number: 2012-14449
Type: Notice
Date: 2012-06-13
Agency: Department of Energy, Federal Energy Regulatory Commission
National Institute on Drug Abuse; Notice of Closed Meetings
Document Number: 2012-14445
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Revisions to the Export Administration Regulations (EAR): Control of Military Training Equipment and Related Items the President Determines No Longer Warrant Control Under the United States Munitions List (USML)
Document Number: 2012-14444
Type: Proposed Rule
Date: 2012-06-13
Agency: Department of Commerce, Bureau of Industry and Security
This proposed rule describes how articles the President determines no longer warrant control under Category IX (Military Training Equipment and Training) of the United States Munitions List (USML) would be controlled under the Commerce Control List (CCL) in new Export Control Classification Numbers (ECCNs) 0A614, 0B614, 0D614, and 0E614. This rule is one in a planned series of proposed rules describing how various types of articles the President determines, as part of the Administration's Export Control Reform Initiative, no longer warrant USML control, would be controlled on the CCL and by the EAR. This proposed rule is being published in conjunction with a proposed rule from the Department of State, Directorate of Defense Trade Controls, which would amend the list of articles enumerated in USML Category IX. The revisions in this rule are part of Commerce's retrospective plan under EO 13563 completed in August 2011. Commerce's full plan can be accessed at: https://open.commerce.gov/news/2011/08/23/commerce-plan- retrospective-analysis-existing-rules.
Amendment to the International Traffic in Arms Regulations: Revision of U.S. Munitions List Category IX
Document Number: 2012-14443
Type: Proposed Rule
Date: 2012-06-13
Agency: Department of State
As part of the President's Export Control Reform effort, the Department of State proposes to amend the International Traffic in Arms Regulations (ITAR) to revise Category IX (military training equipment) of the U.S. Munitions List (USML) to describe more precisely the materials warranting control on the USML. The revisions to this rule are part of the Department of State's retrospective plan under E.O. 13563 completed on August 17, 2011. The Department of State's full plan can be accessed at https:// www.state.gov/documents/organization/181028.pdf.
Ocean Transportation Intermediary License; Applicants
Document Number: 2012-14442
Type: Notice
Date: 2012-06-13
Agency: Federal Maritime Commission, Agencies and Commissions
Ocean Transportation Intermediary License; Revocation
Document Number: 2012-14441
Type: Notice
Date: 2012-06-13
Agency: Federal Maritime Commission, Agencies and Commissions
Political Contributions by Certain Investment Advisers: Ban on Third-Party Solicitation; Extension of Compliance Date
Document Number: 2012-14440
Type: Rule
Date: 2012-06-13
Agency: Securities and Exchange Commission, Agencies and Commissions
The Securities and Exchange Commission (``Commission'' or ``SEC'') is extending the date by which advisers must comply with the ban on third-party solicitation in rule 206(4)-5 under the Investment Advisers Act of 1940, the ``pay to play'' rule. The Commission is extending the compliance date in order to ensure an orderly transition for advisers and third-party solicitors as well as to provide additional time for them to adjust compliance policies and procedures after the transition.
Notice of Agreements Filed
Document Number: 2012-14439
Type: Notice
Date: 2012-06-13
Agency: Federal Maritime Commission, Agencies and Commissions
Proposed Collection; Comment Request: Clinical Mythteries: A Video Game About Clinical Trials
Document Number: 2012-14437
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for opportunity for public comment on proposed data collection projects, the National Institutes of Health (NIH) will publish periodic summaries of proposed projects to be submitted to the Office of Management and Budget (OMB) for review and approval. Proposed Collection: Title: Clinical Mythteries: A Video Game About Clinical Trials. Type of Information Collection Request: NEW. Need and Use of Information Collection: New England Research Institutes as a contractor for the National Heart Lung and Blood Institute is planning to create an engaging, informational ``serious video game'' for adolescents about clinical studies which: (1) Incorporates core learning objectives; and (2) dispels misconceptions. Two types of information collection are planned: usability testing to understand game-play/usability. This information will be collected by focus group and will be digitally recorded 90 minute groups. A pre/post randomized trial to measure change in knowledge. This information will be collected electronically through on-line questionnaire. The game will be incorporated with a larger initiative to provide information about clinical research (https://www.nhlbi.nih.gov/ childrenandclinicalstudies/index.php). Frequency of Response: Once. Affected Public: Individuals. Type of Respondents: Adolescentsaged 8- 14. The annual reporting burden is as follows: Estimated Number of Respondents: 6,148; Estimated Number of Responses per Respondent: 1; Average Burden Hours Per Response: 1.321; and Estimated Total Annual Burden Hours Requested: 370. The annualized cost to respondents is estimated at: $3,700. There are no Capital Costs to report. The Operating Costs to collect this information is estimated at $38,642.
Biennial Progress Report of the Interagency Coordinating Committee on the Validation of Alternative Methods (ICCVAM)
Document Number: 2012-14436
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services
The NTP Interagency Center for the Evaluation of Alternative Toxicological Methods (NICEATM) announces the availability of the Biennial Progress Report 2010-2011: Interagency Coordinating Committee on the Validation of Alternative Methods. The report was prepared in accordance with requirements of the ICCVAM Authorization Act of 2000 (42 U.S.C. 285l-3). The Biennial Progress Report describes activities and progress by NICEATM and ICCVAM during the period from January 2010 through December 2011. During the past two years, NICEATM, ICCVAM, and ICCVAM member agencies contributed to the national and international endorsement and adoption of 14 new and updated alternative safety testing methods. Since ICCVAM was established, NICEATM, ICCVAM, and the ICCVAM member agencies have contributed to the regulatory acceptance of over 50 alternative methods that can be used to protect the health of people, animals, and the environment while reducing, refining, and replacing animal use. The Biennial Progress Report is available on the NICEATM-ICCVAM Web site at https://iccvam.niehs.nih.gov/about/ICCVAMrpts.htm. Copies can also be requested from NICEATM (see ``ADDRESSES'').
Draft Five-Year Plan (2013-2017) for the National Toxicology Program Interagency Center for the Evaluation of Alternative Toxicological Methods and the Interagency Coordinating Committee on the Validation of Alternative Methods
Document Number: 2012-14435
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services
The National Toxicology Program (NTP) Interagency Center for the Evaluation of Alternative Toxicological Methods (NICEATM) in collaboration with the Interagency Coordinating Committee on the Validation of Alternative Methods (ICCVAM) has developed a draft NICEATM-ICCVAM Five-Year Plan. The plan describes four core strategies to foster and promote development, validation, and regulatory acceptance of scientifically sound alternative test methods by the Federal government and by other governments and multinational organizations. This document will provide strategic direction for NICEATM and ICCVAM during 2013-2017. NIEHS and NICEATM request public comments on the draft 2013-2017 Five-Year Plan, which is available at https://iccvam.niehs.nih.gov/docs/ 5yearplan.htm. NICEATM and ICCVAM in partnership with relevant agency program offices will consider these comments during development of the final plan.
Center for Scientific Review; Notice of Closed Meeting
Document Number: 2012-14434
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review; Notice of Closed Meetings
Document Number: 2012-14433
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
National Institute of Arthritis and Musculoskeletal and Skin Diseases; Notice of Closed Meeting
Document Number: 2012-14432
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review; Notice of Closed Meeting
Document Number: 2012-14431
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review; Notice of Closed Meetings
Document Number: 2012-14430
Type: Notice
Date: 2012-06-13
Agency: Department of Health and Human Services, National Institutes of Health
Methyl Bromide; Pesticide Tolerances
Document Number: 2012-14429
Type: Rule
Date: 2012-06-13
Agency: Environmental Protection Agency
This regulation establishes a tolerance for residues of methyl bromide in or on cotton, undelinted seed under the Federal Food, Drug, and Cosmetic Act (FFDCA) because there is a need for imported undelinted cottonseed for use as additional feed for dairy cattle in the United States.
Agency Information Collection Activities: Application for Waiver of the Foreign Residence Requirement of Section 212(e) of the Immigration and Nationality Act; Extension, Without Change of a Currently Approved Collection
Document Number: 2012-14428
Type: Notice
Date: 2012-06-13
Agency: Department of Homeland Security, U.S. Citizenship and Immigration Services
The Department of Homeland Security, U.S. Citizenship and Immigration Services (USCIS) will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and clearance in accordance with the Paperwork Reduction Act of 1995. The information collection notice was previously published in the Federal Register on March 23, 2012, at 77 FR 17085, allowing for a 60-day public comment period. USCIS did not receive any comments in connection with the 60-day notice.
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