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FDA Inspection 876533 — Fresenius Kabi AB

Fresenius Kabi AB — FEI 3002631703

The FDA completed an inspection of Fresenius Kabi AB on April 11, 2014 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 11, 2014
Fiscal Year
2014
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Uppsala (Sweden)

Facility

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  • 1099421 (VAI Tue Oct 16 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1005000 (VAI Tue Feb 07 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources