FDA Warning Letter — Lasik Vision Institute

Case 79178 — FEI 3007726866

The FDA took a Warning Letter action against Lasik Vision Institute on Oct 9, 2009 (Phoenix, AZ). 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
Oct 9, 2009
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Phoenix, AZ (United States)