# FDA Inspection 998381 - Biomet, Inc. - November 22, 2016

Source: https://www.keypedia.com/records/fda_inspections/biomet-inc/e13b0a86-e21c-4b58-a7a4-14f7552987ec
Source feed: FDA_Inspections

> FDA Inspection 998381 for Biomet, Inc. on November 22, 2016. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 998381
- Company Name: Biomet, Inc.
- Inspection Date: 2016-11-22
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/biomet-inc/ca22677e-55e1-4eeb-a8a2-beabeef1c3ad

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