FDA Inspection 1123636 — Dipharma Francis S.r.l.

Dipharma Francis S.r.l. — FEI 3001624853

The FDA completed an inspection of Dipharma Francis S.r.l. on October 25, 2018 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
October 25, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Baranzate (Italy)

Additional Details

Mutual Recognition Agreement (MRA)