FDA Warning Letter — Lasik Vision Institute

Case 215574 — FEI 3008985101

The FDA took a Warning Letter action against Lasik Vision Institute on December 16, 2011 (Bellevue, WA). 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
December 16, 2011
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Bellevue, WA (United States)