FDA Warning Letter — The Lasik Vision Institute

Case 79166 — FEI 3007630430

The FDA took a Warning Letter action against The Lasik Vision Institute on Oct 9, 2009 (Carmel, IN). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
The Lasik Vision Institute
Date
Oct 9, 2009
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Carmel, IN (United States)