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withdrawn,object_id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-0031-0001,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; Availability,Notice,NAD-Notice of Availability of Data,2008-01-30T05:00:00Z,2008,1,2008-01-30T05:00:00Z,2009-01-31T04:59:59Z,2024-11-12T04:09:45Z,E8-01557,1,0,09000064803a4a6b
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