# Surgalign Spine Technologies – FDA Inspection, Oct 25, 2018

Source: https://www.keypedia.com/records/fda_inspections/surgalign-spine-technologies/d604f21b-6926-4e0a-8f51-e2b1646935b8
Source feed: FDA_Inspections

> FDA inspection 1070465 of Surgalign Spine Technologies, October 25, 2018. 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: 1070465
- Company Name: Surgalign Spine Technologies
- Inspection Date: 2018-10-25
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 857986 - 2013-12-03](https://www.keypedia.com/records/fda_inspections/surgalign-spine-technologies/77044457-798b-4eef-b813-7f291284edaa)
- FDA Inspection 637602 - 2010-01-05

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/andrew-j-garufi/567f6aaa-f6f2-45a3-9a58-80b33f3ad021)

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