FDA Inspection 1319490 — Aionex, Inc.
The FDA completed an inspection of Aionex, Inc. on May 6, 2026 in Madison, TN. 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
- May 6, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Madison, TN (United States)