FDA Inspection 711913 — Cambrex Karlskoga AB

Cambrex Karlskoga AB — FEI 3001686607

The FDA completed an inspection of Cambrex Karlskoga AB on February 3, 2011 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
February 3, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Karlskoga (Sweden)