documents: FDA-2009-D-0137-0009

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-D-0137-0009 FDA FDA-2009-D-0137 Reference 26 - "Guidance for Industry: Biological Product Deviation Reporting for Blood and Plasma Establishments, October 2006" - [re FDA-2009-D-0137-0002] Supporting & Related Material REF-Reference (internal unless indicated) 2009-03-30T04:00:00Z 2009 3     2011-06-29T19:45:14Z   0 0 090000648092ff42

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