documents: FDA-2016-N-3818-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2016-N-3818-0001 | FDA | FDA-2016-N-3818 | Content and Format of Substantial Equivalence Reports; Food and Drug Administration Actions on Substantial Equivalence Reports | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2019-04-02T04:00:00Z | 2019 | 4 | 2019-04-02T04:00:00Z | 2019-07-18T03:59:59Z | 2019-07-19T01:00:36Z | 2019-05787 | 0 | 0 | 0900006483b571a6 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref