FDA Inspection 589820 — Dipharma Francis S.r.l.

Dipharma Francis S.r.l. — FEI 3001624853

The FDA completed an inspection of Dipharma Francis S.r.l. on May 15, 2009 in Baranzate. 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
May 15, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Baranzate (Italy)