# FDA Inspection 1048880 - Cutting Edge Spine - December 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/cutting-edge-spine/f5dabd1f-652b-4deb-81ef-d30556f21f2d
Source feed: FDA_Inspections

> FDA Inspection 1048880 for Cutting Edge Spine on December 14, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1048880
- Company Name: Cutting Edge Spine
- Inspection Date: 2017-12-14
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/cutting-edge-spine/5e17f11f-f611-4d66-b492-3625d345e05e

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