FDA Inspection 1119036 — Dipharma Francis S.R.L.

Dipharma Francis S.R.L. — FEI 3003270894

The FDA completed an inspection of Dipharma Francis S.R.L. on Feb 8, 2019 in Caronno Pertusella. 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
Feb 8, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Caronno Pertusella (Italy)

Additional Details

Mutual Recognition Agreement (MRA)