FDA Warning Letter — TLC Laser Eye Centers

Case 79174 — FEI 3007603809

The FDA took a Warning Letter action against TLC Laser Eye Centers on Oct 9, 2009 (Rockville, MD). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
TLC Laser Eye Centers
Date
Oct 9, 2009
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Rockville, MD (United States)