FDA Inspection 599940 — Lasik Vision Institute

Lasik Vision Institute — FEI 3007726866

The FDA completed an inspection of Lasik Vision Institute on Jun 30, 2009 in Phoenix, AZ. 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 30, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Phoenix, AZ (United States)