FDA Inspection 1126904 — Dipharma Francis Srl

Dipharma Francis Srl — FEI 3002806810

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

Additional details

Mutual Recognition Agreement (MRA)

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