Laboratoire Aguettant FDA Record
Laboratoire Aguettant has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Laboratoire Aguettant" is on file.
- Latest inspection
- Nov 6, 2018 · VAI
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 | 1 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Nov 6, 2018 | Champagne, France | Drugs | Voluntary Action Indicated (VAI) | 3014641959 |
- 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 3014641959 | Champagne, France | 1 | Nov 6, 2018 |
Laboratoire Aguettant and the FDA: common questions
Has Laboratoire Aguettant received an FDA warning letter?
No FDA warning letter addressed to the name "Laboratoire Aguettant" 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 Laboratoire Aguettant received an FDA Form 483?
FDA has not published a Form 483 for "Laboratoire Aguettant" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Laboratoire Aguettant?
The most recent FDA inspection on file ended Nov 6, 2018 at Champagne, France and was classified VAI. FDA has 1 inspection of Laboratoire Aguettant on file.
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