FDA Inspection 1055655 — Refocus Group, Inc.

Refocus Group, Inc. — FEI 3004561466

The FDA completed an inspection of Refocus Group, Inc. on May 24, 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 24, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Irving, TX (United States)

Additional Details

Sponsor, Contract Research Organization