FDA Inspection 917907 — Corden Pharma Brussels SA

Corden Pharma Brussels SA — FEI 3002807851

The FDA completed an inspection of Corden Pharma Brussels SA on February 27, 2015 in Brussels. 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
February 27, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brussels (Belgium)