FDA Inspection 1126904 — Dipharma Francis Srl

Dipharma Francis Srl — FEI 3002806810

The FDA completed an inspection of Dipharma Francis Srl on April 20, 2018 in Mereto Di Tomba. 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
April 20, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mereto Di Tomba (Italy)

Additional Details

Mutual Recognition Agreement (MRA)