documents: FDA-2012-F-0138-0012
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2012-F-0138-0012 | FDA | FDA-2012-F-0138 | Reference 4 - Memorandum from A. Khan, Toxicology Review Group, Division of Petition Review, to J. Kidwell, Regulatory Group I, Division of Petition Review, February 11, 2014 re Food Additives Permitted for Direct Addition to Food for Human Consumption; Vitamin D3 | Supporting & Related Material | Background Material | 2014-08-12T04:00:00Z | 2014 | 8 | 2014-08-12T16:12:36Z | 0 | 0 | 090000648181c285 |
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- 0 rows from regs_document_id in fr_regs_crossref