FDA Inspection 980185 — US IOL, Inc
The FDA completed an inspection of US IOL, Inc on Jun 8, 2016 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
- Jun 8, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Lexington, KY (United States)