FDA Inspection 1070920 — Corden Pharma Bergamo SPA

Corden Pharma Bergamo SPA — FEI 3002806963

The FDA completed an inspection of Corden Pharma Bergamo SPA on Sep 27, 2018 in Treviglio. 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)
End Date
Sep 27, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Treviglio (Italy)