FDA Inspection 694809 — KU Leuven Research & Development

KU Leuven Research & Development — FEI 3008520055

The FDA completed an inspection of KU Leuven Research & Development on Sep 16, 2010 in Leuven. 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
Sep 16, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Leuven (Belgium)