FDA Inspection 856392 — Corden Pharma Bergamo SPA

Corden Pharma Bergamo SPA — FEI 3002806963

The FDA completed an inspection of Corden Pharma Bergamo SPA on Nov 8, 2013 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
Nov 8, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Treviglio (Italy)