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FDA Inspection
•Surgalign Spine Technologies•October 25, 2018

Surgalign Spine Technologies – FDA Inspection, Oct 25, 2018

Record Details

This FDA Inspection record concerns Surgalign Spine Technologies, with an inspection on October 25, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Surgalign Spine Technologies
Inspection Date
October 25, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Andrew J. Garufi (Issuing Officer)
View Company Profile

ID · d604f21b-6926-4e0a-8f51-e2b1646935b8

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1070465
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Surgalign Spine Technologies

2
DateClassificationOfficeProject area
December 3, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
January 5, 2010NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Surgalign Spine Technologies
  • FDA Inspection 857986 - 2013-12-03
  • FDA Inspection 637602 - 2010-01-05

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