FDA Inspection 1012457 — AEGIS Spine, Inc.
The FDA completed an inspection of AEGIS Spine, Inc. on May 18, 2017 in Costa Mesa, CA. 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
- May 18, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Costa Mesa, CA (United States)