FDA Warning Letter — Alma Lasers, Inc.

Case 394413 — FEI 3004450661

The FDA took a Warning Letter action against Alma Lasers, Inc. on June 7, 2013 (Buffalo Grove, IL). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Alma Lasers, Inc.
Date
June 7, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Buffalo Grove, IL (United States)