FDA Warning Letter — Sunbeam Products, Inc.

Case 353519 — FEI 1043899

The FDA took a Warning Letter action against Sunbeam Products, Inc. on December 4, 2012 (Atlanta, GA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Sunbeam Products, Inc.
Date
December 4, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Atlanta, GA (United States)