FDA Inspection 928354 — Southern Spine, LLC

Southern Spine, LLC — FEI 3006110997

The FDA completed an inspection of Southern Spine, LLC on April 29, 2015 in Macon, GA. 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
April 29, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Macon, GA (United States)