FDA Warning Letter — Curae'Lase, Inc.

Case 192032 — FEI 3005535133

The FDA took a Warning Letter action against Curae'Lase, Inc. on December 9, 2011 (Loris, SC). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Curae'Lase, Inc.
Date
December 9, 2011
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Loris, SC (United States)