FDA Inspection 1337228 — KU Leuven Research & Development

KU Leuven Research & Development — FEI 3008520055

The FDA completed an inspection of KU Leuven Research & Development on Feb 13, 2025 in Leuven. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 13, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Leuven (Belgium)

Additional Details

Mutual Recognition Agreement (MRA)