FDA Warning Letter — LCA Vision, Inc

Case 79171 — FEI 3007624990

The FDA took a Warning Letter action against LCA Vision, Inc on Oct 9, 2009 (Maple Grove, MN). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
LCA Vision, Inc
Date
Oct 9, 2009
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Maple Grove, MN (United States)