{"database": "openregs", "table": "dockets", "rows": [["FDA-2003-P-0334", "FDA", "Stay the Effective Date of FDA's Determination That Premarket Approval is not Required for a Recombinant Endotoxin Tests Intended for Endotoxin Testing of Human Drugs and Medical Devices; CLOSED: 10/5/2011", "Nonrulemaking", "2021-09-01T01:03:09Z", "0b00006480495eda"]], "columns": ["id", "agency_id", "title", "docket_type", "last_modified", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2003-P-0334"], "units": {}, "query_ms": 14.577343012206256, "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"}