FDA Inspection 705342 — Dipharma Francis Srl

Dipharma Francis Srl — FEI 3002806810

The FDA completed an inspection of Dipharma Francis Srl on December 20, 2010 in Mereto Di Tomba. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 20, 2010
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mereto Di Tomba (Italy)