documents: FDA-2008-D-0031-0002

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0031-0002 FDA FDA-2008-D-0031 Guidance for Industry and Food and Drug Administration Staff; Clinical Laboratory Improvement Amendments of 1988: Recommendations for Clinical Laboratory Improvement Amendments of 1988: Waiver Applications for Manufacturers of In Vitro Diagnostic Devices; Guidance Other GDL-Guidance 2008-01-30T05:00:00Z 2008 1     2011-04-08T19:11:19Z   0 0 09000064803a4c07

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