FDA Inspection 970706 — Revision Optics Inc

Revision Optics Inc — FEI 3005956347

The FDA completed an inspection of Revision Optics Inc on April 22, 2016 in Lake Forest, CA. 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
April 22, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Lake Forest, CA (United States)