FDA Inspection 1063879 — Delpharm Milano Srl

Delpharm Milano Srl — FEI 3003716872

The FDA completed an inspection of Delpharm Milano Srl on May 12, 2017 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
May 12, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Segrate (Italy)

Additional Details

Mutual Recognition Agreement (MRA)