KUBLI FRERES FDA Record
KUBLI FRERES has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "KUBLI FRERES" is on file.
- Latest inspection
- Jan 20, 2012 · 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 |
|---|---|---|---|---|
| Jan 20, 2012 | Morangis, France | Food/Cosmetics | Voluntary Action Indicated (VAI) | 3004274663 |
- 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 3004274663 | Morangis, France | 1 | Jan 20, 2012 |
KUBLI FRERES and the FDA: common questions
Has KUBLI FRERES received an FDA warning letter?
No FDA warning letter addressed to the name "KUBLI FRERES" 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 KUBLI FRERES received an FDA Form 483?
FDA has not published a Form 483 for "KUBLI FRERES" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect KUBLI FRERES?
The most recent FDA inspection on file ended Jan 20, 2012 at Morangis, France and was classified VAI. FDA has 1 inspection of KUBLI FRERES on file.
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