FDA Warning Letter — LASIK Vision Institute LLC

Case 89784 — FEI 3007692135

The FDA took a Warning Letter action against LASIK Vision Institute LLC on February 12, 2010 (West Chester, OH). 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 LLC
Date
February 12, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
West Chester, OH (United States)