FDA Inspection 1177245 — Eurofins Pharmaceutical Product Testing Belgium NV
The FDA completed an inspection of Eurofins Pharmaceutical Product Testing Belgium NV on Aug 2, 2019 in Nazareth. 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
- Aug 2, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Nazareth (Belgium)
Additional details
Mutual Recognition Agreement (MRA)