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withdrawn,object_id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-2026-N-3098-0001,FDA,FDA-2026-N-3098,Agency Information Collection Activities; Proposed Collection; Comment Request; Postmarketing Adverse Experience Reporting,Notice,60 Day Proposed Information Collection,2026-05-13T04:00:00Z,2026,5,2026-05-13T04:00:00Z,2026-07-14T03:59:59Z,2026-05-13T16:56:28Z,2026-09543,1,0,09000064b92d4966