AAK Sweden AB — FDA Facility Profile

FEI 3007981449

AAK Sweden AB is an FDA-registered facility (FEI 3007981449) located in Karlshamn, SE. Registered operations: API MANUFACTURE. RegDataLab tracks 3 FDA inspections at this facility.

Facility Details

Location
Karlshamn (SE)
Registration Expires
December 31, 2026
Operations
API MANUFACTURE
Source
decrs