FDA Inspection 1314334 — Spine Wave, Inc.
The FDA completed an inspection of Spine Wave, Inc. on April 21, 2026 in Shelton, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- April 21, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Shelton, CT (United States)