Danipharm A/S — FDA Facility Profile

FEI 3002806781

Danipharm A/S is an FDA-registered facility (FEI 3002806781) located in NIBE, DK. Registered operations: API MANUFACTURE. RegDataLab tracks 4 FDA inspections at this facility.

Facility Details

Location
NIBE (DK)
Registration Expires
December 31, 2026
Operations
API MANUFACTURE
Source
decrs