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.

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Facility Details

Location
Karlshamn (SE)
Registration Expires
Dec 31, 2027
Operations
API MANUFACTURE
Source
decrs

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.