FDA Inspection 1093792 — SPINE INNOVATION, LLC
The FDA completed an inspection of SPINE INNOVATION, LLC on Apr 30, 2019 in Del Mar, 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
- Apr 30, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Del Mar, CA (United States)