FDA Inspection 637602 — Surgalign Spine Technologies
The FDA completed an inspection of Surgalign Spine Technologies on Jan 5, 2010 in Deerfield, IL. 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
- Jan 5, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Deerfield, IL (United States)