FDA Inspection 705342 — Dipharma Francis Srl

Dipharma Francis Srl — FEI 3002806810

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

Inspection details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.