FDA Inspection 1208591 — Corden Pharma Bergamo SPA

Corden Pharma Bergamo SPA — FEI 3002806963

The FDA completed an inspection of Corden Pharma Bergamo SPA on Mar 18, 2022 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
Mar 18, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Treviglio (Italy)

Additional Details

Mutual Recognition Agreement (MRA)