EDELMONT FDA Record
- Latest inspection NAI · Sep 12, 2019
- No warning letters matched by name
EDELMONT has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "EDELMONT" is on file.
- Latest inspection
- Sep 12, 2019 · NAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 11, 2026 (checked Nov 15, 2026, unchanged) | File dated Nov 10, 2026 | Current |
| 510(k) clearances | 0 | Nov 15, 2026 | File dated Nov 9, 2026 | Current |
| Inspections | 1 | Nov 15, 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 |
|---|---|---|---|---|
| Sep 12, 2019 | La Balme De Thuy, France | Food/Cosmetics | No Action Indicated (NAI) | 3003490632 |
- 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 3003490632 | La Balme De Thuy, France | 1 | Sep 12, 2019 |
EDELMONT and the FDA: common questions
Has EDELMONT received an FDA warning letter?
No FDA warning letter addressed to the name "EDELMONT" 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 EDELMONT received an FDA Form 483?
FDA has not published a Form 483 for "EDELMONT" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect EDELMONT?
The most recent FDA inspection on file ended Sep 12, 2019 at La Balme De Thuy, France and was classified NAI. FDA has 1 inspection of EDELMONT on file.
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