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withdrawn,object_id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-2011-N-0231-0008,FDA,FDA-2011-N-0231,Agency Information Collection Activities; Proposed Collection; Comment Request; Adverse Experience Reporting for Licensed Biological Products; and General Records,Notice,60 Day Proposed Information Collection,2017-07-18T04:00:00Z,2017,7,2017-07-18T04:00:00Z,2017-09-19T03:59:59Z,2023-09-07T21:06:37Z,2017-15004,0,0,090000648293b6b2