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withdrawn,object_id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-2016-N-2544-0002,FDA,FDA-2016-N-2544,"Agency Information Collection Activities; Submission for Office of
Management and Budget Review; Comment Request; Medical Device:
Current Good Manufacturing Practice Quality System Regulations",Notice,30 Day Proposed Information Collection,2016-12-05T05:00:00Z,2016,12,2016-12-05T05:00:00Z,2017-01-05T04:59:59Z,2016-12-05T16:16:22Z,2016-29028,0,0,09000064823dedfc
FDA-2016-N-2544-0001,FDA,FDA-2016-N-2544,Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Device: Current Good Manufacturing Practice Quality System Regulations,Notice,60 Day Proposed Information Collection,2016-09-08T04:00:00Z,2016,9,2016-09-08T04:00:00Z,2016-11-08T04:59:59Z,2016-09-08T13:22:12Z,2016-21553,0,0,09000064821e0ce0