Eurofins BioPharma Product Testing Leiden B.V. — FDA Facility Profile
Eurofins BioPharma Product Testing Leiden B.V. is an FDA-registered facility (FEI 3004594563) located in South Holland 2333 CR, NL. Registered operations: ANALYSIS. RegDataLab tracks 5 FDA inspections at this facility.
Facility Details
- Location
- South Holland 2333 CR (NL)
- Registration Expires
- December 31, 2026
- Operations
- ANALYSIS
- Source
- decrs