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FDA Inspection
•Spine Wave, Inc.•April 25, 2023

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

Record Details

This FDA Inspection record concerns Spine Wave, Inc., with an inspection on April 25, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
Spine Wave, Inc.
Inspection Date
April 25, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Katarzyna Plona
View Company Profile

ID · c07e8114-e8fd-4c7c-bfd9-edd98dd9352a

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1203863
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Spine Wave, Inc.

4
DateClassificationOfficeProject area
April 21, 2026NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
January 10, 2017NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 24, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
September 3, 2009NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Spine Wave, Inc.
  • FDA Inspection 1314334 - 2026-04-21
  • FDA Inspection 997070 - 2017-01-10
  • FDA Inspection 833623 - 2013-05-24
  • FDA Inspection 611259 - 2009-09-03

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