Menicon Pharma SAS FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

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.

What these totals cover: FDA records filed under the name "Menicon Pharma SAS" and its spelling variant "Menicon Pharma". Records filed under related names are not included; see Related names.

Latest inspection
Aug 22, 2012 · NAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections1Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent FDA inspections

1 inspection on Aug 22, 2012.

DateSiteProductClassificationFEI
Aug 22, 2012Illkirch Graffenstaden, FranceDevicesNo 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.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3003779166Illkirch Graffenstaden, France1Aug 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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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.