FDA Warning Letter — Lasik Vision Institute

Case 104266 — FEI 3007628644

The FDA took a Warning Letter action against Lasik Vision Institute on April 20, 2010 (Boca Raton, FL). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Lasik Vision Institute
Date
April 20, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Boca Raton, FL (United States)