documents: FDA-2006-N-0040-0002
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2006-N-0040-0002 | FDA | FDA-2006-N-0040 | Draft Regulatory Action for Review to OMB and OIRA re: Requirements for Human Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use Part 1 of 2 | Supporting & Related Material | Background Material | 2007-11-13T05:00:00Z | 2007 | 11 | 2016-02-24T15:32:22Z | 0 | 0 | 0900006480442292 |
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- 0 rows from regs_document_id in fr_regs_crossref