Synthon s.r.o. — FDA Facility Profile

FEI 3005212485

Synthon s.r.o. is an FDA-registered facility (FEI 3005212485) located in Czech Republic (CZE). Registered operations: ANALYSIS; API MANUFACTURE. RegDataLab tracks 4 FDA inspections at this facility.

Facility Details

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