FDA Inspection 857590 — Delpharm Milano Srl

Delpharm Milano Srl — FEI 3003716872

The FDA completed an inspection of Delpharm Milano Srl on Sep 19, 2013 in Segrate. 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
Sep 19, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Segrate (Italy)

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