documents: FDA-2011-N-0231-0011
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-0231-0011 | 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 | 2020-09-01T04:00:00Z | 2020 | 9 | 2020-09-01T04:00:00Z | 2020-11-03T04:59:59Z | 2023-09-07T21:08:45Z | 2020-19239 | 0 | 0 | 090000648482d8bb |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref