# Spine Wave, Inc. – FDA Inspection, Jan 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/spine-wave-inc/b53caa8b-e706-4a96-86c8-c7cf92eb0949
Source feed: FDA_Inspections

> FDA inspection 997070 of Spine Wave, Inc., January 10, 2017. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 997070
- Company Name: Spine Wave, Inc.
- Inspection Date: 2017-01-10
- 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: 2

## Related Documents

- FDA Inspection 1314334 - 2026-04-21
- [FDA Inspection 1203863 - 2023-04-25](https://www.keypedia.com/records/fda_inspections/spine-wave-inc/c07e8114-e8fd-4c7c-bfd9-edd98dd9352a)
- FDA Inspection 833623 - 2013-05-24
- FDA Inspection 611259 - 2009-09-03

## Related Officers

- [Company Rep](https://www.keypedia.com/people/michael-g-mayfield/ec045e12-d940-4f76-a17f-98ba4a8dd5b9)

Company: https://www.keypedia.com/companies/spine-wave-inc/0db78bd2-56ee-41d2-b916-66111cff70a2

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