documents: FDA-2013-N-1439-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2013-N-1439-0001 | FDA | FDA-2013-N-1439 | Agency Information Collection Activities; Proposed Collection; Comment Request; Adverse Event Program for Medical Products | Notice | General Notice | 2013-11-29T05:00:00Z | 2013 | 11 | 2013-11-29T05:00:00Z | 2014-01-29T04:59:59Z | 2013-11-29T17:16:39Z | 2013-28600 | 0 | 0 | 090000648149f214 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref