FDA Inspection 819585 — Corden Pharma Brussels SA

Corden Pharma Brussels SA — FEI 3002807851

The FDA completed an inspection of Corden Pharma Brussels SA on January 30, 2013 in Brussels. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 30, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brussels (Belgium)