# Surgalign Spine Technologies – FDA Inspection, Dec 3, 2013

Source: https://www.keypedia.com/records/fda_inspections/surgalign-spine-technologies/77044457-798b-4eef-b813-7f291284edaa
Source feed: FDA_Inspections

> FDA inspection 857986 of Surgalign Spine Technologies, December 03, 2013. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 857986
- Company Name: Surgalign Spine Technologies
- Inspection Date: 2013-12-03
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1070465 - 2018-10-25](https://www.keypedia.com/records/fda_inspections/surgalign-spine-technologies/d604f21b-6926-4e0a-8f51-e2b1646935b8)
- FDA Inspection 637602 - 2010-01-05

Company: https://www.keypedia.com/companies/surgalign-spine-technologies/d947dfd9-9a9a-4c6e-a3dc-edd8aebfe019

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7