FDA Inspection 594209 — The Lasik Vision Institute

The Lasik Vision Institute — FEI 3007630430

The FDA completed an inspection of The Lasik Vision Institute on Jun 15, 2009 in Carmel, IN. 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 15, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Carmel, IN (United States)