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 Mar 14, 2017 in Baranzate. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

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

Additional details

Mutual Recognition Agreement (MRA)

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