FDA Inspection 1181739 — Optego Vision USA, Inc.

Optego Vision USA, Inc. — FEI 1000160574

The FDA completed an inspection of Optego Vision USA, Inc. on Aug 24, 2022 in Tucson, 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
Aug 24, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Tucson, AZ (United States)