# FDA Inspection 596100 - Biomet UK Ltd. - July 02, 2009

Source: https://www.keypedia.com/records/fda_inspections/biomet-uk-ltd/c46b5fcd-d3fe-484d-bc2f-5154ea127caf
Source feed: FDA_Inspections

> FDA Inspection 596100 for Biomet UK Ltd. on July 02, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 596100
- Company Name: Biomet UK Ltd.
- Inspection Date: 2009-07-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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