FDA Inspection 1071932 — Summit Spine LLC

Summit Spine LLC — FEI 3011145476

The FDA completed an inspection of Summit Spine LLC on Oct 10, 2018 in Georgetown, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 10, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Georgetown, TX (United States)