FDA Inspection 1054737 — Refocus Group, Inc.

Refocus Group, Inc. — FEI 3004561466

The FDA completed an inspection of Refocus Group, Inc. on May 3, 2018 in Irving, 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
May 3, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Irving, TX (United States)