documents: FDA-2013-D-0636-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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| FDA-2013-D-0636-0001 | FDA | FDA-2013-D-0636 | Global Unique Device Identification Database; Draft Guidance for Industry; Availability | Notice | Notice of Availability | 2013-09-24T04:00:00Z | 2013 | 9 | 2013-09-24T04:00:00Z | 2013-11-26T04:59:59Z | 2013-11-30T21:24:11Z | 2013-23058 | 0 | 0 | 090000648143435c |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref