{"database": "openregs", "table": "documents", "rows": [["FDA-2010-N-0621-0193", "FDA", "FDA-2010-N-0621", "Genentech, Inc. (Covington & Burling LLP) to the Presiding Officer (Karen Midthun, M.D.), June 13, 2011 - Letter", "Other", "Letter(s)", "2011-06-16T04:00:00Z", 2011, 6, "2011-06-16T04:00:00Z", null, "2013-08-11T03:15:21Z", null, 0, 0, "0900006480e4f82f"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2010-N-0621-0193"], "units": {}, "query_ms": 1.112945843487978, "source": "Federal Register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"}