FDA Inspection 1273764 — Cambrex Karlskoga AB

Cambrex Karlskoga AB — FEI 3001686607

The FDA completed an inspection of Cambrex Karlskoga AB on May 24, 2024 in Karlskoga. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 24, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Karlskoga (Sweden)

Additional Details

Mutual Recognition Agreement (MRA)