FDA Inspection 1067545 — Sunbeam Products, Inc.

Sunbeam Products, Inc. — FEI 1043899

The FDA completed an inspection of Sunbeam Products, Inc. on August 23, 2018 in Atlanta, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 23, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Atlanta, GA (United States)