FDA Inspection 584458 — Corden Pharma Brussels SA

Corden Pharma Brussels SA — FEI 3002807851

The FDA completed an inspection of Corden Pharma Brussels SA on Apr 2, 2009 in Brussels. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Apr 2, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brussels (Belgium)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.