{"database": "openregs", "table": "documents", "rows": [["FDA-2005-N-0161-0007", "FDA", "FDA-2005-N-0161", "Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Current Good Manufacturing Practices and Related Regulations for Blood and Blood\nComponents; and Requirements for Donor Testing, Donor Notification, and \u2018\u2018Lookback\u2019\u2019", "Notice", "30 Day Proposed Information Collection", "2015-03-03T05:00:00Z", 2015, 3, "2015-03-03T05:00:00Z", "2015-04-03T03:59:59Z", "2025-07-02T17:20:41Z", "2015-04381", 0, 0, "0900006481a26cb7"]], "columns": ["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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2005-N-0161-0007"], "units": {}, "query_ms": 0.3104470670223236, "source": "Federal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"}