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FDA Inspection 1064287 — 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 July 26, 2018 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
July 26, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Swindon (United Kingdom)

Facility

Other inspections at this 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))
  • 1051240 (NAI Thu Sep 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 990487 (VAI Tue Sep 06 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources