FDA Inspection 662765 — Fareva Amboise

Fareva Amboise — FEI 3000234005

The FDA completed an inspection of Fareva Amboise on April 29, 2010 in Poce Sur Cisse. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 29, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Poce Sur Cisse (France)