# Welbilt U.K. Ltd – FDA Inspection, Apr 25, 2018

Source: https://www.keypedia.com/records/fda_inspections/welbilt-uk-ltd/9b3d4ea9-0f06-408b-a2d4-0841411ca8e3
Source feed: FDA_Inspections

> FDA inspection 1050400 of Welbilt U.K. Ltd, April 25, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 1030. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1050400
- Company Name: Welbilt U.K. Ltd
- Inspection Date: 2018-04-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1187346 - 2022-11-04](https://www.keypedia.com/records/fda_inspections/welbilt-uk-ltd/90cfcfc4-b791-4cbf-9828-f2ceabd8cc79)
- [FDA Inspection 970669 - 2016-04-27](https://www.keypedia.com/records/fda_inspections/welbilt-uk-ltd/cb0e0b26-e70c-48fe-a491-9fd0058f9920)

## Related Officers

- Issuing Officer
- Issuing Officer

Company: https://www.keypedia.com/companies/welbilt-uk-ltd/241c7bee-acec-41a0-a873-29c8d7eff132

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7