# FDA Inspection 961922 - Nexus Spine, LLC - February 23, 2016

Source: https://www.keypedia.com/records/fda_inspections/nexus-spine-llc/11cea676-e2ba-473f-969e-d431c275f17b
Source feed: FDA_Inspections

> FDA Inspection 961922 for Nexus Spine, LLC on February 23, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 961922
- Company Name: Nexus Spine, LLC
- Inspection Date: 2016-02-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/nexus-spine-llc/21b5e28f-cb11-4437-bfe2-975cc6f320fc

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