FDA Inspection 1080822 — FUSION ORTHOPEDICS USA

FUSION ORTHOPEDICS USA — FEI 3013365802

The FDA completed an inspection of FUSION ORTHOPEDICS USA on Dec 21, 2018 in Mesa, AZ. 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
Dec 21, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mesa, AZ (United States)