Eurofins Biopharma Product Testing, Denmark A/S — FDA Facility Profile

FEI 3006272083

Eurofins Biopharma Product Testing, Denmark A/S is an FDA-registered facility (FEI 3006272083) located in Hovedstaden DK-2600, DK. Registered operations: ANALYSIS. RegDataLab tracks 5 FDA inspections at this facility.

Facility Details

Location
Hovedstaden DK-2600 (DK)
Registration Expires
December 31, 2026
Operations
ANALYSIS
Source
decrs