{"database": "openregs", "table": "dockets", "rows": [["FDA-2005-P-0436", "FDA", "take the administrative action of clarifying, in writing,whether or not the dietary supplement VI-28 TM, as detailed in the pre-market notification filed 18 August 2005, upon importation into the US, shall be deemed adulterated under 402(f) take the administrative action of clarifying, in writing, whether or not the dietary supplment VI-28 TM, as detailed in the pre-market notification filed 18 Au", "Nonrulemaking", "2021-09-01T01:01:29Z", "0b0000648045043a"]], "columns": ["id", "agency_id", "title", "docket_type", "last_modified", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2005-P-0436"], "units": {}, "query_ms": 0.3842099104076624, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}