# Centinel Spine, Inc. – FDA Inspection, May 19, 2010

Source: https://www.keypedia.com/records/fda_inspections/centinel-spine-inc/aa4ba258-d2a4-4c3f-9453-19f2c0d3bb9d
Source feed: FDA_Inspections

> FDA inspection 668019 of Centinel Spine, Inc., May 19, 2010. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 668019
- Company Name: Centinel Spine, Inc.
- Inspection Date: 2010-05-19
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1079097 - 2018-04-05](https://www.keypedia.com/records/fda_inspections/centinel-spine-inc/7bd1137a-181e-44ec-a24e-9a473b377b4b)
- FDA Inspection 814780 - 2013-01-15

Company: https://www.keypedia.com/companies/centinel-spine-inc/0cf88b41-f7f6-4276-a12e-1b60f8b17a48

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