Menicon Pharma SAS FDA Record
Menicon Pharma SAS has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Menicon Pharma SAS" is on file.
- Latest inspection
- Aug 22, 2012 · 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 | 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 |
|---|---|---|---|---|
| Aug 22, 2012 | Illkirch Graffenstaden, France | Devices | No Action Indicated (NAI) | 3003779166 |
- 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 3003779166 | Illkirch Graffenstaden, France | 1 | Aug 22, 2012 |
Menicon Pharma SAS and the FDA: common questions
Has Menicon Pharma SAS received an FDA warning letter?
No FDA warning letter addressed to the name "Menicon Pharma SAS" 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 Menicon Pharma SAS received an FDA Form 483?
FDA has not published a Form 483 for "Menicon Pharma SAS" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Menicon Pharma SAS?
The most recent FDA inspection on file ended Aug 22, 2012 at Illkirch Graffenstaden, France and was classified NAI. FDA has 1 inspection of Menicon Pharma SAS on file.
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