documents: FDA-2008-D-0611-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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| FDA-2008-D-0611-0001 | FDA | FDA-2008-D-0611 | Draft Guidance for Industry and Food and Drug Administration Staff; Submission and Review of Sterility Information in Premarket Notification Submissions for Devices Labeled as Sterile; Availability | Notice | NAD-Notice of Availability of Data | 2008-12-12T05:00:00Z | 2008 | 12 | 2008-12-12T05:00:00Z | 2009-03-13T03:59:59Z | 2009-03-19T21:37:24Z | E8-29413 | 0 | 0 | 09000064807d8787 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref