# Biomet U.K., Ltd. – FDA Inspection, Feb 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/biomet-uk-ltd/e2638e2b-51ac-46ac-af16-c79752c152ef
Source feed: FDA_Inspections

> FDA inspection 1085654 of Biomet U.K., Ltd., February 14, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1085654
- Company Name: Biomet U.K., Ltd.
- Inspection Date: 2019-02-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

Company: https://www.keypedia.com/companies/biomet-uk-ltd/ec4429c5-eed0-46ae-a92c-0d6119315ecf

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