FDA Inspection 662765 — Fareva Amboise

Fareva Amboise — FEI 3000234005

The FDA completed an inspection of Fareva Amboise on Apr 29, 2010 in Poce Sur Cisse. 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
Apr 29, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Poce Sur Cisse (France)

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