FDA Inspection 1020853 — Unified Spine, Llc

Unified Spine, Llc — FEI 3006215390

The FDA completed an inspection of Unified Spine, Llc on July 6, 2017 in Westerville, OH. 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
July 6, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Westerville, OH (United States)