documents
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
5 rows where docket_id = "FDA-2010-D-0605" sorted by posted_date descending
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Suggested facets: subtype, open_for_comment, posted_date (date), comment_start_date (date), last_modified (date)
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2010-D-0605-0004 | FDA | None FDA-2010-D-0605 | Reference 2 - FDA. Report a Problem. How to Report Problems With Products Regulated by FDA, http://www.fda.gov/AboutFDA/ContactFDA/ReportaProblem/default.htm. | Supporting & Related Material | GDL-Guidance | 2010-12-16T05:00:00Z | 2010 | 12 | 2010-12-16T20:15:49Z | 0 | 0 | 0900006480bb894b | |||
| FDA-2010-D-0605-0002 | FDA | None FDA-2010-D-0605 | Guidance for Industry; Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements Small Entiy Compliance Guide | Other | Guidance | 2010-12-16T05:00:00Z | 2010 | 12 | 2010-12-16T05:00:00Z | 2024-11-07T22:29:06Z | 1 | 0 | 0900006480bb8335 | ||
| FDA-2010-D-0605-0003 | FDA | None FDA-2010-D-0605 | Reference 1 - FDA. Guidance for Industry: Product Recalls, Including Removals and Corrections, http://www.fda.gov/Safety/Recalls/IndustryGuidance/ucm129259.htm | Supporting & Related Material | GDL-Guidance | 2010-12-16T05:00:00Z | 2010 | 12 | 2010-12-16T20:15:47Z | 0 | 0 | 0900006480bb8949 | |||
| FDA-2010-D-0605-0001 | FDA | None FDA-2010-D-0605 | Small Entity Compliance Guides; Availability, etc.: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements | Notice | NAD-Notice of Availability of Data | 2010-12-16T05:00:00Z | 2010 | 12 | 2010-12-16T05:00:00Z | 2024-11-12T05:00:25Z | 2010-31613 | 1 | 0 | 0900006480bb8272 | |
| FDA-2010-D-0605-0005 | FDA | None FDA-2010-D-0605 | Reference 3 - FDA. Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act, http://www.fda.gov/FoodGuidances | Supporting & Related Material | GDL-Guidance | 2010-12-16T05:00:00Z | 2010 | 12 | 2010-12-16T20:15:51Z | 0 | 0 | 0900006480bb894d |
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CREATE TABLE documents (
id TEXT PRIMARY KEY,
agency_id TEXT,
docket_id TEXT REFERENCES dockets(id),
title TEXT,
document_type TEXT,
subtype TEXT,
posted_date TEXT,
posted_year INTEGER,
posted_month INTEGER,
comment_start_date TEXT,
comment_end_date TEXT,
last_modified TEXT,
fr_doc_num TEXT,
open_for_comment INTEGER,
withdrawn INTEGER,
object_id TEXT
);
CREATE INDEX idx_docs_agency ON documents(agency_id);
CREATE INDEX idx_docs_docket ON documents(docket_id);
CREATE INDEX idx_docs_date ON documents(posted_date);
CREATE INDEX idx_docs_year ON documents(posted_year);
CREATE INDEX idx_docs_type ON documents(document_type);
CREATE INDEX idx_docs_frnum ON documents(fr_doc_num);
CREATE INDEX idx_docs_comment_end ON documents(comment_end_date) WHERE comment_end_date IS NOT NULL AND withdrawn = 0;