# FDA Inspection 918449 - Spinal Kinetics Inc - March 18, 2015

Source: https://www.keypedia.com/records/fda_inspections/spinal-kinetics-inc/c3999ff7-1ecb-49c1-bf8d-abe8fb260af3
Source feed: FDA_Inspections

> FDA Inspection 918449 for Spinal Kinetics Inc on March 18, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 918449
- Company Name: Spinal Kinetics Inc
- Inspection Date: 2015-03-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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- [FDA Inspection 803510 - 2012-10-17](https://www.keypedia.com/records/fda_inspections/spinal-kinetics-inc/60f7e137-a2ed-4ae7-a16a-b1a28f04fc75)

Company: https://www.keypedia.com/companies/spinal-kinetics-inc/5e130b58-958d-475d-839c-017207eacf80

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