FDA Inspection 1331890 — Slow Wave, Inc.
The FDA completed an inspection of Slow Wave, Inc. on Aug 4, 2026 in Lakeway, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 4, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lakeway, TX (United States)