Dr. Brown's Company FDA Record
Dr. Brown's Company has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Dr. Brown's Company" is on file.
- Latest inspection
- Mar 11, 2025 · NAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 5 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Reviewing Dr. Brown's Company as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Or check Dr. Brown's Company yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.
Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Mar 11, 2025 | Saint Louis, MO | Food/Cosmetics | No Action Indicated (NAI) | 3017929998 |
| Oct 31, 2013 | Saint Louis, MO | Devices | Voluntary Action Indicated (VAI) | 3008138005 |
| Oct 31, 2013 | Bonne Terre, MO | Devices | Voluntary Action Indicated (VAI) | 3008819945 |
| Feb 23, 2011 | Saint Louis, MO | Devices | No Action Indicated (NAI) | 3008138005 |
| Feb 23, 2011 | Bonne Terre, MO | Devices | No Action Indicated (NAI) | 3008819945 |
- NAI
- No objectionable conditions or practices were found during the inspection.
- VAI
- Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
- OAI
- Regulatory and/or administrative actions are recommended.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3017929998 | Saint Louis, MO | 1 | Mar 11, 2025 |
| FEI 3008138005 | Saint Louis, MO | 2 | Oct 31, 2013 |
| FEI 3008819945 | Bonne Terre, MO | 2 | Oct 31, 2013 |
Dr. Brown's Company and the FDA: common questions
Has Dr. Brown's Company received an FDA warning letter?
No FDA warning letter addressed to the name "Dr. Brown's Company" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has Dr. Brown's Company received an FDA Form 483?
FDA has not published a Form 483 for "Dr. Brown's Company" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Dr. Brown's Company?
The most recent FDA inspection on file ended Mar 11, 2025 at Saint Louis, MO and was classified NAI. FDA has 5 inspections of Dr. Brown's Company on file.
Need more than this page shows? Ask about Dr. Brown's Company in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.