FDA Inspection 650548 — 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 11, 2010 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 11, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Caronno Pertusella (Italy)