documents: FDA-2008-D-0610-0008

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2008-D-0610-0008 FDA FDA-2008-D-0610 Draft Guidance for Industry; Availability Postmarketing Adverse Event Reporting for Medical Products and Dietary Supplements During an Influenza Pandemic Notice NAD-Notice of Availability of Data 2011-01-07T05:00:00Z 2011 1 2011-01-07T05:00:00Z 2011-03-09T04:59:59Z 2011-03-03T20:47:47Z 2011-00094 0 0 0900006480bc6d37

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