FDA Inspection 871282 — Dipharma Francis Srl

Dipharma Francis Srl — FEI 3002806810

The FDA completed an inspection of Dipharma Francis Srl on March 7, 2014 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
March 7, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mereto Di Tomba (Italy)