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withdrawn,object_id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-2003-N-0251-0007,FDA,FDA-2003-N-0251,Supporting Statement for Medical Devices; Inspection by Accredited Persons Program,Supporting & Related Material,Background Material,2003-12-09T05:00:00Z,2003,12,,,2025-02-25T12:58:27Z,,0,0,090000648048f645
FDA-2003-N-0251-0008,FDA,FDA-2003-N-0251,"Agency Information Collection Activities; Announcement of the Office of Management and Budget Approval; Inspection by Accredited Persons Program Under the Medical Device User Fee and Modernization Act of
2002",Notice,General Notice,2003-12-09T05:00:00Z,2003,12,,,2025-02-25T12:43:16Z,03-30534,0,0,090000648048f647
FDA-2003-N-0251-0006,FDA,FDA-2003-N-0251,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Inspection by Accredited Persons Program Under the Medical Device User Fee and Modernization Act of 2002,Notice,30 Day Proposed Information Collection,2003-10-15T04:00:00Z,2003,10,2003-10-08T04:00:00Z,2003-11-08T04:59:59Z,2025-02-25T12:37:49Z,03-25444,0,0,090000648048f642
FDA-2003-N-0251-0003,FDA,FDA-2003-N-0251,Supporting Statement for Medical Devices; Inspection by Accredited Persons Program,Supporting & Related Material,Background Material,2003-07-08T04:00:00Z,2003,7,,,2025-02-25T12:50:07Z,,0,0,090000648048f63b
FDA-2003-N-0251-0005,FDA,FDA-2003-N-0251,Supporting Statement for Medical Devices; Inspection by Accredited Persons Program,Supporting & Related Material,Background Material,2003-07-08T04:00:00Z,2003,7,,,2025-02-25T12:56:11Z,,0,0,090000648048f640
FDA-2003-N-0251-0004,FDA,FDA-2003-N-0251,Supporting Statement for Medical Devices; Inspection by Accredited Persons Program,Supporting & Related Material,Background Material,2003-07-08T04:00:00Z,2003,7,,,2025-02-25T12:52:20Z,,0,0,090000648048f63e
FDA-2003-N-0251-0002,FDA,FDA-2003-N-0251,Agency Information Collection Activities; Announcement of OMB Approval; Inspection by Accredited Persons Program Under the Medical Device User Fee and Modernization Act of 2002,Notice,Notice of Approval,2003-07-01T04:00:00Z,2003,7,,,2025-02-25T12:31:08Z,03-16110,0,0,090000648048f626
FDA-2003-N-0251-0001,FDA,FDA-2003-N-0251,Agency Emergency Processing Under OMB Review; Inspection by Accredited Persons Program Under the Medical Device User Fee and Modernization Act of 2002,Notice,General Notice,2003-05-01T04:00:00Z,2003,5,2003-04-28T04:00:00Z,2003-05-29T03:59:59Z,2025-02-25T12:27:20Z,03-10414,0,0,090000648048f5ef