documents: FDA-2012-N-1067-0010
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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| FDA-2012-N-1067-0010 | FDA | FDA-2012-N-1067 | Reference 2 - FDA, ``Draft Guidance for Industry #232: Studies to Evaluate the Safety of Residues of Veterinary Drugs in Human Food: General Approach to Establish an Acute Reference Dose (ARfD) re New Animal Drugs; Updating Tolerances for Residues of New Animal Drugs in Food | Supporting & Related Material | Background Material | 2016-10-28T04:00:00Z | 2016 | 10 | 2016-10-28T13:46:28Z | 0 | 0 | 090000648235b041 |
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