FDA Inspection 924743 — 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 6, 2015 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
May 6, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Baranzate (Italy)