documents: FDA-2011-N-0231-0009
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-0231-0009 | FDA | FDA-2011-N-0231 | Agency Information Collection Activities; Submission for Office of Management and Budget Review; Adverse Experience Reporting for Licensed Biological Products; and General Records | Notice | 30 Day Proposed Information Collection | 2018-01-08T05:00:00Z | 2018 | 1 | 2018-01-08T05:00:00Z | 2018-02-08T04:59:59Z | 2023-09-07T21:06:53Z | 2018-00095 | 0 | 0 | 0900006482db13e0 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref