FDA Inspection 1238177 — Fresenius Kabi AB

Fresenius Kabi AB — FEI 3002631703

The FDA completed an inspection of Fresenius Kabi AB on April 21, 2023 in Uppsala. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 21, 2023
Fiscal Year
2023
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Uppsala (Sweden)

Additional Details

Mutual Recognition Agreement (MRA)