FDA Inspection 802559 — US IOL, Inc

US IOL, Inc — FEI 1037089

The FDA completed an inspection of US IOL, Inc on October 9, 2012 in Lexington, KY. 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
October 9, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Lexington, KY (United States)