# Biomet UK Ltd. – FDA Inspection, Aug 3, 2017

Source: https://www.keypedia.com/records/fda_inspections/biomet-uk-ltd/b538dbaf-9862-45ce-ac1e-985b4db1db1f
Source feed: FDA_Inspections

> FDA inspection 1021429 of Biomet UK Ltd., August 03, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021429
- Company Name: Biomet UK Ltd.
- Inspection Date: 2017-08-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1222658 - 2023-11-02](https://www.keypedia.com/records/fda_inspections/biomet-uk-ltd/43e3f384-0592-4baf-b59e-936e985736a6)
- [FDA Inspection 918189 - 2015-03-18](https://www.keypedia.com/records/fda_inspections/biomet-uk-ltd/3d51f05b-b53d-4b91-9606-3f38956b203c)
- FDA Inspection 596100 - 2009-07-02

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/thai-t-duong/59737092-2f30-43a7-b23b-36fa7f212c4a)

Company: https://www.keypedia.com/companies/biomet-uk-ltd/721bcb54-1ff5-4a79-9d08-bb0bed5fccae

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