FDA Inspection 955765 — Revision Optics Inc

Revision Optics Inc — FEI 3005956347

The FDA completed an inspection of Revision Optics Inc on February 2, 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
February 2, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Lake Forest, CA (United States)

Additional Details

Sponsor, Contract Research Organization