FDA Inspection 912110 — Ethypharm

Ethypharm — FEI 3004715600

The FDA completed an inspection of Ethypharm on Dec 5, 2014 in Le Grand Quevilly CEDEX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Dec 5, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Le Grand Quevilly CEDEX (France)

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