# Vertebral Technologies, Inc. – FDA Inspection, Nov 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/vertebral-technologies-inc/91b487da-9ff3-434c-bdef-4c7428d5be70
Source feed: FDA_Inspections

> FDA inspection 994689 of Vertebral Technologies, Inc., November 16, 2016. Classification: No Action Indicated (NAI). 3 citations under 21 CFR parts 806 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 994689
- Company Name: Vertebral Technologies, Inc.
- Inspection Date: 2016-11-16
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 912320 - 2015-02-02](https://www.keypedia.com/records/fda_inspections/vertebral-technologies-inc/4e21fed2-8b41-450a-a86d-b1876a004bad)
- FDA Inspection 776625 - 2012-04-16
- FDA Inspection 588231 - 2009-06-12

## Related Officers

- [Company Rep](https://www.keypedia.com/people/jennifer-s-ness/532f8a81-e393-4e83-b5f2-a72362e966de)

Company: https://www.keypedia.com/companies/vertebral-technologies-inc/136ed3a9-e2ed-492a-9c70-30d12953740f

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