FDA Inspection 1071928 — Zynex Medical, Inc.

Zynex Medical, Inc. — FEI 3000214920

The FDA completed an inspection of Zynex Medical, Inc. on October 30, 2018 in Englewood, CO. 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
October 30, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Englewood, CO (United States)