FDA Warning Letter — Syneron, Inc.

Case 135834 — FEI 3004772125

The FDA took a Warning Letter action against Syneron, Inc. on Dec 23, 2010 (Irvine, CA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Syneron, Inc.
Date
Dec 23, 2010
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Irvine, CA (United States)