FDA Inspection 1237790 — IntelleWave, Inc.
The FDA completed an inspection of IntelleWave, Inc. on April 25, 2024 in New Port Richey, FL. 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 25, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- New Port Richey, FL (United States)