Cross-Media Electronic Reporting: Authorized Program Revision Approval, Commonwealth of Virginia, 17255-17256 [2017-07145]

Download as PDF Federal Register / Vol. 82, No. 67 / Monday, April 10, 2017 / Notices Agency’s receipt of the requests for voluntary cancellations and/or amendments to terminate uses of products listed in Tables 1 and 2 of Unit II. IV. Cancellation Order Pursuant to FIFRA section 6(f) (7 U.S.C. 136d(f)(1)), EPA hereby approves the requested cancellations and/or amendments to terminate uses of the registrations identified in Tables 1 and 2 of Unit II. Accordingly, the Agency hereby orders that the product registrations identified in Tables 1 and 2 of Unit II. are canceled and/or amended to terminate the affected uses. The effective date of the propoxur product cancellations that are subject to this notice is December 31, 2017. The effective date of the remaining cancellations that are subject to this notice is April 10, 2017. Any distribution, sale, or use of existing stocks of the products identified in Tables 1 and 2 of Unit II. in a manner inconsistent with any of the provisions for disposition of existing stocks set forth in Unit VI. will be a violation of FIFRA. asabaliauskas on DSK3SPTVN1PROD with NOTICES V. What is the agency’s authority for taking this action? Section 6(f)(1) of FIFRA (7 U.S.C. 136d(f)(1)) provides that a registrant of a pesticide product may at any time request that any of its pesticide registrations be canceled or amended to terminate one or more uses. FIFRA further provides that, before acting on the request, EPA must publish a notice of receipt of any such request in the Federal Register. Thereafter, following the public comment period, the EPA Administrator may approve such a request. The notice of receipt for this action was published for comment in the Federal Register of November 22, 2016 (81 FR 83833) (FRL–9954–80). The comment period closed on December 22, 2016. VI. Provisions for Disposition of Existing Stocks Existing stocks are those stocks of registered pesticide products which are currently in the United States and which were packaged, labeled, and released for shipment prior to the effective date of the action. The existing stocks provisions for the products subject to this order are as follows: A. For Propoxur Products 279–3395, 3862–135, 6218–24, 11556–33, 89459– 28, 89459–39 Identified in Table 1 of Unit II. At the request of the registrant FMC Corporation, the effective product VerDate Sep<11>2014 20:02 Apr 07, 2017 Jkt 241001 cancelation date for the propoxur products listed in Table 1 of Unit II. is December 31, 2017. The registrants may continue to sell and distribute existing stocks of the propoxur products listed in Table 1 of Unit II. until December 31, 2017. Thereafter, registrants will be prohibited from selling or distributing the propoxur products identified in Table 1 of Unit II., except for export consistent with FIFRA section 17 (7 U.S.C. 136o) or for proper disposal. Persons other than the registrant may sell, distribute, or use existing stocks of the affected cancelled products until supplies are exhausted, provided that such sale, distribution, or use is consistent with the terms of the previously approved labeling on, or that accompanied, the cancelled products. B. For All Other Products Identified in Table 1 and 2 of Unit II. For all other voluntary product cancellations noted, the registrants may continue to sell and distribute existing stocks of products listed in Table 1 of Unit II. until April 10, 2018, which is 1 year after publication of this cancellation order in the Federal Register. Thereafter, registrants are prohibited from selling or distributing the products identified in Table 1 of Unit II., except for export consistent with FIFRA section 17 (7 U.S.C. 136o) or for proper disposal. In the case of products for which there are requested amendments to terminate uses, once EPA has approved product labels reflecting the requested amendments to terminate uses, the registrant will be permitted to sell or distribute products under the previously approved labeling for a period of 18 months after the date of Federal Register publication of the cancellation order, unless other restrictions have been imposed. Thereafter, the registrant will be prohibited from selling or distributing the products whose labels include the deleted uses identified in Table 2 of Unit II., except for export consistent with FIFRA section 17 or for proper disposal. Persons other than the registrant may sell, distribute, or use existing stocks of the affected cancelled products/ products under the previously approved labeling until supplies are exhausted, provided that such sale, distribution, or use is consistent with the terms of the previously approved labeling on, or that accompanied, the cancelled products/ products under the previously approved labeling. Authority: 7 U.S.C. 136 et seq. PO 00000 Frm 00078 Fmt 4703 Sfmt 4703 17255 Dated: March 9, 2017. Yu-Ting Guilaran, Director, Pesticide Re-Evaluation Division, Office of Pesticide Programs. [FR Doc. 2017–07133 Filed 4–7–17; 8:45 am] BILLING CODE 6560–50–P ENVIRONMENTAL PROTECTION AGENCY [FRL_9957–03–OEI] Cross-Media Electronic Reporting: Authorized Program Revision Approval, Commonwealth of Virginia Environmental Protection Agency (EPA). ACTION: Notice. AGENCY: This notice announces EPA’s approval of the Commonwealth of Virginia’s request to revise its National Primary Drinking Water Regulations Implementation EPA-authorized program to allow electronic reporting. DATES: EPA’s approval is effective May 10, 2017 for the Commonwealth of Virginia’s National Primary Drinking Water Regulations Implementation program, if no timely request for a public hearing is received and accepted by the Agency. FOR FURTHER INFORMATION CONTACT: Karen Seeh, U.S. Environmental Protection Agency, Office of Environmental Information, Mail Stop 2823T, 1200 Pennsylvania Avenue NW., Washington, DC 20460, (202) 566–1175, seeh.karen@epa.gov. SUPPLEMENTARY INFORMATION: On October 13, 2005, the final Cross-Media Electronic Reporting Rule (CROMERR) was published in the Federal Register (70 FR 59848) and codified as part 3 of title 40 of the CFR. CROMERR establishes electronic reporting as an acceptable regulatory alternative to paper reporting and establishes requirements to assure that electronic documents are as legally dependable as their paper counterparts. Subpart D of CROMERR requires that state, tribal or local government agencies that receive, or wish to begin receiving, electronic reports under their EPA-authorized programs must apply to EPA for a revision or modification of those programs and obtain EPA approval. Subpart D provides standards for such approvals based on consideration of the electronic document receiving systems that the state, tribe, or local government will use to implement the electronic reporting. Additionally, § 3.1000(b) through (e) of 40 CFR part 3, subpart D provides special procedures for program revisions and modifications to allow SUMMARY: E:\FR\FM\10APN1.SGM 10APN1 asabaliauskas on DSK3SPTVN1PROD with NOTICES 17256 Federal Register / Vol. 82, No. 67 / Monday, April 10, 2017 / Notices electronic reporting, to be used at the option of the state, tribe or local government in place of procedures available under existing programspecific authorization regulations. An application submitted under the subpart D procedures must show that the state, tribe or local government has sufficient legal authority to implement the electronic reporting components of the programs covered by the application and will use electronic document receiving systems that meet the applicable subpart D requirements. Once an authorized program has EPA’s approval to accept electronic documents under certain programs, CROMERR § 3.1000(a)(4) requires that the program keep EPA apprised of any changes to laws, policies, or the electronic document receiving systems that have the potential to affect the program’s compliance with CROMERR § 3.2000. On January 27, 2017, the Virginia Department of Health (VDH) submitted an amended application titled Compliance Monitoring Data Portal for revision to its EPA-approved drinking water program under title 40 CFR to allow new electronic reporting. EPA reviewed VDH’s request to revise its EPA-authorized program and, based on this review, EPA determined that the application met the standards for approval of authorized program revision/modification set out in 40 CFR part 3, subpart D. In accordance with 40 CFR 3.1000(d), this notice of EPA’s decision to approve Virginia’s request to revise its Part 142—National Primary Drinking Water Regulations Implementation program to allow electronic reporting under 40 CFR part 141 is being published in the Federal Register. VDH was notified of EPA’s determination to approve its application with respect to the authorized program listed above. Also, in today’s notice, EPA is informing interested persons that they may request a public hearing on EPA’s action to approve the Commonwealth of Virginia’s request to revise its authorized public water system program under 40 CFR part 142, in accordance with 40 CFR 3.1000(f). Requests for a hearing must be submitted to EPA within 30 days of publication of today’s Federal Register notice. Such requests should include the following information: (1) The name, address and telephone number of the individual, organization or other entity requesting a hearing; (2) A brief statement of the requesting person’s interest in EPA’s determination, a brief explanation as to why EPA should hold a hearing, and VerDate Sep<11>2014 20:02 Apr 07, 2017 Jkt 241001 any other information that the requesting person wants EPA to consider when determining whether to grant the request; (3) The signature of the individual making the request, or, if the request is made on behalf of an organization or other entity, the signature of a responsible official of the organization or other entity. In the event a hearing is requested and granted, EPA will provide notice of the hearing in the Federal Register not less than 15 days prior to the scheduled hearing date. Frivolous or insubstantial requests for hearing may be denied by EPA. Following such a public hearing, EPA will review the record of the hearing and issue an order either affirming today’s determination or rescinding such determination. If no timely request for a hearing is received and granted, EPA’s approval of the Commonwealth of Virginia’s request to revise its part 142—National Primary Drinking Water Regulations Implementation program to allow electronic reporting will become effective 30 days after today’s notice is published, pursuant to CROMERR section 3.1000(f)(4). Matthew Leopard, Director, Office of Information Management. [FR Doc. 2017–07145 Filed 4–7–17; 8:45 am] BILLING CODE 6560–50–P ENVIRONMENTAL PROTECTION AGENCY Do not submit electronically any information you consider to be Confidential Business Information (CBI) or other information whose disclosure is restricted by statute. • Mail: OPP Docket, Environmental Protection Agency Docket Center (EPA/ DC), (28221T), 1200 Pennsylvania Ave. NW., Washington, DC 20460–0001. • Hand Delivery: To make special arrangements for hand delivery or delivery of boxed information, please follow the instructions at https:// www.epa.gov/dockets/contacts.html. Additional instructions on commenting or visiting the docket, along with more information about dockets generally, is available at https:// www.epa.gov/dockets. FOR FURTHER INFORMATION CONTACT: Steve Knizner, Antimicrobials Division (AD) (7510P), main telephone number: (703) 305–7090; email address: ADFRNotices@epa.gov., Michael Goodis, Registration Division (RD) (7505P), main telephone number: (703) 305–7090; email address: RDFRNotices@epa.gov. The mailing address for each contact person is: Office of Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460–0001. As part of the mailing address, include the contact person’s name, division, and mail code. The division to contact is listed at the end of each application summary. SUPPLEMENTARY INFORMATION: I. General Information A. Does this action apply to me? You may be potentially affected by Pesticide Product Registration; this action if you are an agricultural Receipt of Applications for New Uses producer, food manufacturer, or pesticide manufacturer. The following AGENCY: Environmental Protection list of North American Industrial Agency (EPA). Classification System (NAICS) codes is ACTION: Notice. not intended to be exhaustive, but rather SUMMARY: EPA has received applications provides a guide to help readers to register new uses of pesticide determine whether this document products containing currently registered applies to them. Potentially affected active ingredients. Pursuant to the entities may include: • Crop production (NAICS code 111). Federal Insecticide, Fungicide, and • Animal production (NAICS code Rodenticide Act (FIFRA), EPA is hereby 112). providing notice of receipt and • Food manufacturing (NAICS code opportunity to comment on these 311). applications. • Pesticide manufacturing (NAICS DATES: Comments must be received on code 32532). or before May 10, 2017. If you have any questions regarding ADDRESSES: Submit your comments, the applicability of this action to a identified by the Docket Identification particular entity, consult the person (ID) Number and the EPA Registration listed under FOR FURTHER INFORMATION Number of interest as shown in the body CONTACT. of this document by one of the following B. What should I consider as I prepare methods: • Federal eRulemaking Portal: https:// my comments for EPA? www.regulations.gov. Follow the online 1. Submitting CBI. Do not submit this instructions for submitting comments. information to EPA through [EPA–HQ–OPP–2017–0007; FRL–9959–60] PO 00000 Frm 00079 Fmt 4703 Sfmt 4703 E:\FR\FM\10APN1.SGM 10APN1

Agencies

[Federal Register Volume 82, Number 67 (Monday, April 10, 2017)]
[Notices]
[Pages 17255-17256]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-07145]


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ENVIRONMENTAL PROTECTION AGENCY

[FRL_9957-03-OEI]


Cross-Media Electronic Reporting: Authorized Program Revision 
Approval, Commonwealth of Virginia

AGENCY: Environmental Protection Agency (EPA).

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: This notice announces EPA's approval of the Commonwealth of 
Virginia's request to revise its National Primary Drinking Water 
Regulations Implementation EPA-authorized program to allow electronic 
reporting.

DATES: EPA's approval is effective May 10, 2017 for the Commonwealth of 
Virginia's National Primary Drinking Water Regulations Implementation 
program, if no timely request for a public hearing is received and 
accepted by the Agency.

FOR FURTHER INFORMATION CONTACT: Karen Seeh, U.S. Environmental 
Protection Agency, Office of Environmental Information, Mail Stop 
2823T, 1200 Pennsylvania Avenue NW., Washington, DC 20460, (202) 566-
1175, seeh.karen@epa.gov.

SUPPLEMENTARY INFORMATION: On October 13, 2005, the final Cross-Media 
Electronic Reporting Rule (CROMERR) was published in the Federal 
Register (70 FR 59848) and codified as part 3 of title 40 of the CFR. 
CROMERR establishes electronic reporting as an acceptable regulatory 
alternative to paper reporting and establishes requirements to assure 
that electronic documents are as legally dependable as their paper 
counterparts. Subpart D of CROMERR requires that state, tribal or local 
government agencies that receive, or wish to begin receiving, 
electronic reports under their EPA-authorized programs must apply to 
EPA for a revision or modification of those programs and obtain EPA 
approval. Subpart D provides standards for such approvals based on 
consideration of the electronic document receiving systems that the 
state, tribe, or local government will use to implement the electronic 
reporting. Additionally, Sec.  3.1000(b) through (e) of 40 CFR part 3, 
subpart D provides special procedures for program revisions and 
modifications to allow

[[Page 17256]]

electronic reporting, to be used at the option of the state, tribe or 
local government in place of procedures available under existing 
program-specific authorization regulations. An application submitted 
under the subpart D procedures must show that the state, tribe or local 
government has sufficient legal authority to implement the electronic 
reporting components of the programs covered by the application and 
will use electronic document receiving systems that meet the applicable 
subpart D requirements. Once an authorized program has EPA's approval 
to accept electronic documents under certain programs, CROMERR Sec.  
3.1000(a)(4) requires that the program keep EPA apprised of any changes 
to laws, policies, or the electronic document receiving systems that 
have the potential to affect the program's compliance with CROMERR 
Sec.  3.2000.
    On January 27, 2017, the Virginia Department of Health (VDH) 
submitted an amended application titled Compliance Monitoring Data 
Portal for revision to its EPA-approved drinking water program under 
title 40 CFR to allow new electronic reporting. EPA reviewed VDH's 
request to revise its EPA-authorized program and, based on this review, 
EPA determined that the application met the standards for approval of 
authorized program revision/modification set out in 40 CFR part 3, 
subpart D. In accordance with 40 CFR 3.1000(d), this notice of EPA's 
decision to approve Virginia's request to revise its Part 142--National 
Primary Drinking Water Regulations Implementation program to allow 
electronic reporting under 40 CFR part 141 is being published in the 
Federal Register.
    VDH was notified of EPA's determination to approve its application 
with respect to the authorized program listed above.
    Also, in today's notice, EPA is informing interested persons that 
they may request a public hearing on EPA's action to approve the 
Commonwealth of Virginia's request to revise its authorized public 
water system program under 40 CFR part 142, in accordance with 40 CFR 
3.1000(f). Requests for a hearing must be submitted to EPA within 30 
days of publication of today's Federal Register notice. Such requests 
should include the following information:
    (1) The name, address and telephone number of the individual, 
organization or other entity requesting a hearing;
    (2) A brief statement of the requesting person's interest in EPA's 
determination, a brief explanation as to why EPA should hold a hearing, 
and any other information that the requesting person wants EPA to 
consider when determining whether to grant the request;
    (3) The signature of the individual making the request, or, if the 
request is made on behalf of an organization or other entity, the 
signature of a responsible official of the organization or other 
entity.
    In the event a hearing is requested and granted, EPA will provide 
notice of the hearing in the Federal Register not less than 15 days 
prior to the scheduled hearing date. Frivolous or insubstantial 
requests for hearing may be denied by EPA. Following such a public 
hearing, EPA will review the record of the hearing and issue an order 
either affirming today's determination or rescinding such 
determination. If no timely request for a hearing is received and 
granted, EPA's approval of the Commonwealth of Virginia's request to 
revise its part 142--National Primary Drinking Water Regulations 
Implementation program to allow electronic reporting will become 
effective 30 days after today's notice is published, pursuant to 
CROMERR section 3.1000(f)(4).

Matthew Leopard,
Director, Office of Information Management.
[FR Doc. 2017-07145 Filed 4-7-17; 8:45 am]
 BILLING CODE 6560-50-P
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