FDA Inspection 1187346 — Welbilt U.K. Ltd

Welbilt U.K. Ltd — FEI 3009845468

The FDA completed an inspection of Welbilt U.K. Ltd on November 4, 2022 in Sheffield. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 4, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Sheffield (United Kingdom)

Citations

IDCFRDescription
503421 CFR 1010.2(c)Certification not based on adequate test/testing program
594021 CFR 1030.10(c)(3)(i)tests--errors and uncertainties accounted for