# FDA Inspection 796934 - Kasios Bone Substitutes - September 06, 2012

Source: https://www.keypedia.com/records/fda_inspections/kasios-bone-substitutes/0bdb633c-227f-4dbb-a65f-a4f86f2218c6
Source feed: FDA_Inspections

> FDA Inspection 796934 for Kasios Bone Substitutes on September 06, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 796934
- Company Name: Kasios Bone Substitutes
- Inspection Date: 2012-09-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/kasios-bone-substitutes/8531ef0b-6e4b-4865-af6e-eb726d7957a2

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