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withdrawn,object_id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-2008-N-0334-0016,FDA,FDA-2008-N-0334,Agency Information Collection Activities; Proposed Collection; Comment Request; Postmarketing Safety Reports for Human Drug and Biological Products: Electronic Submission Requirements,Notice,60 Day Proposed Information Collection,2017-10-30T04:00:00Z,2017,10,2017-10-30T04:00:00Z,2017-12-30T04:59:59Z,2017-10-30T15:50:49Z,2017-23518,0,0,0900006482c21dfe