# Spine Wave, Inc. – FDA Inspection, Apr 25, 2023

Source: https://www.keypedia.com/records/fda_inspections/spine-wave-inc/c07e8114-e8fd-4c7c-bfd9-edd98dd9352a
Source feed: FDA_Inspections

> FDA inspection 1203863 of Spine Wave, Inc., April 25, 2023. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1203863
- Company Name: Spine Wave, Inc.
- Inspection Date: 2023-04-25
- 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 1314334 - 2026-04-21
- [FDA Inspection 997070 - 2017-01-10](https://www.keypedia.com/records/fda_inspections/spine-wave-inc/b53caa8b-e706-4a96-86c8-c7cf92eb0949)
- FDA Inspection 833623 - 2013-05-24
- FDA Inspection 611259 - 2009-09-03

## Related Officers

- [Katarzyna Plona](https://www.keypedia.com/people/katarzyna-plona/ea20d6c6-5d2d-41a0-a755-0647fb9f3250)

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