Eurofins BioPharma Product Testing Czech Republic s.r.o. — FDA Facility Profile

FEI 3008920466

Eurofins BioPharma Product Testing Czech Republic s.r.o. is an FDA-registered facility (FEI 3008920466) located in Czech Republic (CZE). Registered operations: ANALYSIS. RegDataLab tracks 5 FDA inspections at this facility.

Facility Details

Location
Czech Republic (CZE)
Registration Expires
December 31, 2026
Operations
ANALYSIS
Source
decrs