documents: FDA-2011-D-0147-0008
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-D-0147-0008 | FDA | FDA-2011-D-0147 | Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry and Food and Drug Administration Staff; Section 905(j) Reports: Demonstrating Substantial Equivalence for Tobacco Products and Demonstrating the Substantial Equivalence of a New Tobacco Product: Responses to Frequently Asked Questions | Notice | 60 Day Proposed Information Collection | 2015-03-05T05:00:00Z | 2015 | 3 | 2015-03-05T05:00:00Z | 2015-05-05T03:59:59Z | 2024-06-20T23:28:28Z | 2015-05024 | 0 | 0 | 0900006481a2e27c |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref