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withdrawn,object_id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-2004-N-0054-0003,FDA,FDA-2004-N-0054,Medwatch - The FDA Safety Information and Adverse Event Reporting Program (Sample),Supporting & Related Material,Background Material,2004-12-28T05:00:00Z,2004,12,,,2025-09-24T15:16:08Z,,0,0,090000648046e8f8
FDA-2004-N-0054-0002,FDA,FDA-2004-N-0054,Medwatch - The FDA Safety Information and Adverse Event Reporting Program (Sample),Supporting & Related Material,Background Material,2004-12-28T05:00:00Z,2004,12,,,2025-09-24T15:15:44Z,,0,0,090000648046e8f7
FDA-2004-N-0054-0001,FDA,FDA-2004-N-0054,Agency Information Collection Activities; Proposed Collection; Comment Request; MedWatch: Food and Drug Administration Medical Products Reporting Program,Notice,60 Day Proposed Information Collection,2004-12-28T00:00:00Z,2004,12,2004-12-27T05:00:00Z,2005-02-26T04:59:59Z,2025-05-13T09:00:41Z,04-28138,0,0,090000648046e8f4