Normativa EEUUAgo. 26, 2011
Abren plazo para comentarios públicos sobre cargos honorarios bajo la Ley de Modernización de Seguridad Alimentaria
11 August 2011
|Committee on Sanitary and Phytosanitary Measures||Original: English|
The following communication, received on 9 August 2011, is being circulated at the request of the Delegation of the United States.
|Food Safety Modernization Act Domestic and Foreign Facility Reinspections, Recall, and Importer Reinspection User Fee Rates for Fiscal Year 2012|
| The US Food and Drug Administration (FDA) is announcing the fiscal year (FY) 2012 fee rates for certain domestic and foreign facility reinspections, failure to comply with a recall order, and importer reinspections that are mandated in the Federal Food, Drug, and Cosmetic Act (the FD&C Act), amended by the FDA Food Safety Modernization Act (FSMA). These fees are effective on 1 October 2011, and will remain in effect through 30 September 2012. Invoices for these fees for FY 2012 will be issued using the fee schedule established in this document. FDA is accepting comments to this document and intends to consider such comments in implementing these user fees in FY 2013. The notice published in the Federal Register on 1 August 2011 76 FR 45820. The notice can be found at: http://www.gpo.gov/fdsys/pkg/FR-2011-08-01/pdf/2011-19331.pdf.
FDA recognizes that there is significant international interest in how we are implementing the Food Safety Modernization Act of 2010, and as a result has elected to is notify this action to give US trading partners an opportunity to submit comments on the burden of fee amounts on small business, even though this notification is not an obligation under Article 7, Annex B.
|This addendum concerns a:|
|[ ] Modification of final date for comments|
|[ ] Notification of adoption, publication or entry into force of regulation|
|[ ] Modification of content and/or scope of previously notified draft regulation|
|[ ] Withdrawal of proposed regulation|
|[ ] Change in proposed date of adoption, publication or date of entry into force|
|[X] Other: Notice for public comment on fee burdens under the FDA Food Safety Modernization Act (FSMA)|
|Comment period: (If the addendum extends the scope of the previously notified measure in terms of products and/or potentially affected Members, a new deadline for receipt of comments should be provided, normally of at least 60 calendar days. Under other circumstances, such as extension of originally announced final date for comments, the comment period provided in the addendum may vary.)|
|[ ] Sixty days from the date of circulation of the addendum to the notification and/or (dd/mm/yy): 31 October 2011|
|Agency or authority designated to handle comments: [ ] National Notification Authority, [ ] National Enquiry Point. Address, fax number and e-mail address (if available) of other body:|
|Submit electronic comments to http://www.regulations.gov. Submit written comments to the Division of Dockets Management (HFA-305). Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. Please indicate Docket No. FDA-2011-N-0528 with comment submission.
For further information contact: Amy Waltrip, 12420 Parklawn Dr., Rm. 2012, Rockville, MD 20857, 1-301-796-8811, E-mail: Amy.Waltrip@fda.hhs.gov
|Text available from: [X] National Notification Authority, [ ] National Enquiry Point. Address, fax number and e-mail address (if available) of other body:|
|United States SPS National Notification Authority, USDA Foreign Agricultural Service, International Regulations and Standards Division (IRSD), Stop 1014, Washington D.C. 20250; Tel: +(1 202) 720 1301; Fax: +(1 202) 720 0433; E-mail: email@example.com
Text available on the internet at: http://www.gpo.gov/fdsys/pkg/FR-2011-08-01/pdf/2011-19331.pdf