FDA Inspection 857590 — Delpharm Milano Srl

Delpharm Milano Srl — FEI 3003716872

The FDA completed an inspection of Delpharm Milano Srl on September 19, 2013 in Segrate. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 19, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Segrate (Italy)