FDA Inspection 589820 — 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 15, 2009 in Baranzate. 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
May 15, 2009
Fiscal Year
2009
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.