FDA Inspection 924743 — Dipharma Francis S.R.L.

Dipharma Francis S.R.L. — FEI 3001624853

The FDA completed an inspection of Dipharma Francis S.R.L. on May 6, 2015 in Baranzate. 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
May 6, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Baranzate (Italy)

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