# FDA Inspection 598579 - SpineMatrix Inc - August 27, 2009

Source: https://www.keypedia.com/records/fda_inspections/spinematrix-inc/7315a080-0736-41bc-afd2-bbbf9198d275
Source feed: FDA_Inspections

> FDA Inspection 598579 for SpineMatrix Inc on August 27, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 598579
- Company Name: SpineMatrix Inc
- Inspection Date: 2009-08-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 661569 - 2010-05-07](https://www.keypedia.com/records/fda_inspections/spinematrix-inc/d4a8b9f9-db08-42d7-a815-2ca371dffbf6)
- [FDA Inspection 598579 - 2009-08-27](https://www.keypedia.com/records/fda_inspections/spinematrix-inc/8e9a3352-f8c7-4f91-92a3-977f92d1f2ae)

Company: https://www.keypedia.com/companies/spinematrix-inc/7fe8828c-952a-4c87-990b-9c7a780890ab

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