documents: FDA-2009-N-0114-0003

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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id agency_id docket_id title document_type subtype posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2009-N-0114-0003 FDA FDA-2009-N-0114 Tab A - "Draft Regulatory Action , May 5, 2010" - [OMB Review, EO12866, RPMS Note to the DDM, May 5, 2010 - (Implementation of Device Registration and Listing Requirements Enacted in Section 321 of the Public Health Security and Bioterrorism Preparedness and Response Act of 2002, and Title II of the FDAAA 2007; Proposed Rule, March 26, 2010) - Reference] re FDA-2009-N-0114-0002 Supporting & Related Material REF-Reference (internal unless indicated) 2010-05-18T04:00:00Z 2010 5     2011-06-11T16:28:04Z   0 0 0900006480ae7fb9

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