FDA Inspection 1102910 — US IOL, Inc

US IOL, Inc — FEI 1037089

The FDA completed an inspection of US IOL, Inc on Aug 28, 2019 in Lexington, KY. 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 28, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Lexington, KY (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.