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FDA Inspection 990487 — Catalent U.K. Swindon Zydis Limited

Catalent U.K. Swindon Zydis Limited — FEI 3003812585

The FDA completed an inspection of Catalent U.K. Swindon Zydis Limited on September 6, 2016 in Swindon. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 6, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Swindon (United Kingdom)

Facility

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  • 1261182 (VAI Thu Jun 15 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1141164 (VAI Thu Feb 20 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1064287 (VAI Thu Jul 26 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1051240 (NAI Thu Sep 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources