FDA Inspection 1065698 — Dipharma Francis S.r.l.

Dipharma Francis S.r.l. — FEI 3001624853

The FDA completed an inspection of Dipharma Francis S.r.l. on March 14, 2017 in Baranzate. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 14, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Baranzate (Italy)

Additional Details

Mutual Recognition Agreement (MRA)