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withdrawn,object_id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-2001-N-0105-0003,FDA,FDA-2001-N-0105,"Agency Information Collection Activities; Announcement of OMB Approval; Medical Devices; Third-Party Premarket Submission Review and
Quality System Inspections Under United States/European Community Mutual Recognition Agreement",Notice,Notice of Approval,2002-04-02T05:00:00Z,2002,4,,,2025-02-03T15:00:13Z,02-7526,0,0,09000064804bafed
FDA-2001-N-0105-0002,FDA,FDA-2001-N-0105,Agency Information Collection Activities; Submission for OMB Review; Comment Request; Medical Devices; Third-Party Premarket Submission Review and Quality System Inspections Under United States/European Community Mutual Recognition Agreement,Notice,30 Day Proposed Information Collection,2002-01-14T05:00:00Z,2002,1,2002-01-14T05:00:00Z,2002-02-14T04:59:59Z,2025-02-03T14:55:57Z,02-854,0,0,09000064804bafe5