FDA Inspection 1263511 — Avertix Medical, Inc.
The FDA completed an inspection of Avertix Medical, Inc. on March 11, 2025 in Eatontown, NJ. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- March 11, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Eatontown, NJ (United States)