FDA Inspection 802559 — US IOL, Inc
The FDA completed an inspection of US IOL, Inc on Oct 9, 2012 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
- Oct 9, 2012
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lexington, KY (United States)