FDA Inspection 795216 — Menicon Pharma SAS

Menicon Pharma SAS — FEI 3003779166

The FDA completed an inspection of Menicon Pharma SAS on Aug 22, 2012 in Illkirch Graffenstaden. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Aug 22, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Illkirch Graffenstaden (France)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.