# FDA Inspection 579982 - Biomet 3i, LLC - May 01, 2009

Source: https://www.keypedia.com/records/fda_inspections/biomet-3i-llc/82c588f9-e6d1-4e3c-9ff8-f3d4a1fde8fc
Source feed: FDA_Inspections

> FDA Inspection 579982 for Biomet 3i, LLC on May 01, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 579982
- Company Name: Biomet 3i, LLC
- Inspection Date: 2009-05-01
- Classification: Voluntary Action Indicated (VAI)
- 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-3i-llc/c989df4d-fea7-4593-bb08-6a3362c62250

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