FDA Inspection
Surgalign Spine TechnologiesSurgalign Spine Technologies – FDA Inspection, Dec 3, 2013
Record Details
This FDA Inspection record concerns Surgalign Spine Technologies, with an inspection on December 3, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Surgalign Spine Technologies
- Inspection Date
- December 3, 2013
- Product Type
- Devices
View Company Profile
ID · 77044457-798b-4eef-b813-7f291284edaa
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 857986
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Surgalign Spine Technologies
2| Date | Classification | Office | Project area |
|---|---|---|---|
| October 25, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 5, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Surgalign Spine Technologies
- FDA Inspection 1070465 - 2018-10-25
- FDA Inspection 637602 - 2010-01-05
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