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withdrawn,object_id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-0031-0008,FDA,FDA-2008-D-0031,"Agency Information Collection Activities; Announcement of Office of
Management and Budget Approvals",Notice,Information Collection Request (ICR),2019-11-07T05:00:00Z,2019,11,2019-11-07T05:00:00Z,,2019-11-07T14:57:47Z,2019-24263,0,0,09000064841282a4
FDA-2008-D-0031-0007,FDA,FDA-2008-D-0031,"Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Clinical Laboratory Improvement Amendments Waiver
Applications",Notice,30 Day Proposed Information Collection,2019-07-25T04:00:00Z,2019,7,2019-07-25T04:00:00Z,2019-08-27T03:59:59Z,2019-07-25T13:35:29Z,2019-15787,0,0,0900006483db6304
FDA-2008-D-0031-0006,FDA,FDA-2008-D-0031,Agency Information Collection Activities; Proposed Collection; Comment Request; Clinical Laboratory Improvement Amendments Waiver Applications,Notice,60 Day Proposed Information Collection,2019-03-26T04:00:00Z,2019,3,2019-03-26T04:00:00Z,2019-05-29T03:59:59Z,2019-03-26T13:47:22Z,2019-05759,0,0,0900006483b2e215
FDA-2008-D-0031-0005,FDA,FDA-2008-D-0031,"Agency Information Collection Activities; Proposals, Submissions, and Approvals: Announcement of Office of Management and Budget Approvals",Notice,Notice of Approval,2016-12-19T05:00:00Z,2016,12,2016-12-19T05:00:00Z,,2016-12-19T15:45:42Z,2016-30351,0,0,09000064824264d0
FDA-2008-D-0031-0004,FDA,FDA-2008-D-0031,"Agency Information Collection Activities; Submission for Office of
Management and Budget Review; Comment Request; Clinical Laboratory
Improvement Amendments Act of 1988
Waiver Applications",Notice,30 Day Proposed Information Collection,2016-07-18T04:00:00Z,2016,7,2016-07-18T04:00:00Z,2016-08-18T03:59:59Z,2016-07-18T15:07:32Z,2016-16886,0,0,09000064820bffd1
FDA-2008-D-0031-0003,FDA,FDA-2008-D-0031,"Agency Information Collection Activities; Proposed Collection; Comment Request; Clinical Laboratory Improvement Amendments Act of 1988
Waiver Applications",Notice,60 Day Proposed Information Collection,2016-04-01T04:00:00Z,2016,4,2016-04-01T04:00:00Z,2016-06-01T03:59:59Z,2016-04-01T13:51:11Z,2016-07365,0,0,0900006481f09393
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