# Sunbeam Products, Inc. – FDA Inspection, Jun 28, 2013

Source: https://www.keypedia.com/records/fda_inspections/sunbeam-products-inc/31c929ab-d35c-48ed-a952-17399aca081a
Source feed: FDA_Inspections

> FDA inspection 839700 of Sunbeam Products, Inc., June 28, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 839700
- Company Name: Sunbeam Products, Inc.
- Inspection Date: 2013-06-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1067545 - 2018-08-23
- [FDA Inspection 933679 - 2015-06-19](https://www.keypedia.com/records/fda_inspections/sunbeam-products-inc/39e75980-907d-436b-9353-0892def7bb8f)
- [FDA Inspection 793902 - 2012-08-03](https://www.keypedia.com/records/fda_inspections/sunbeam-products-inc/b3c46255-728b-4708-8f37-60b42388be92)
- [FDA Inspection 625873 - 2009-10-30](https://www.keypedia.com/records/fda_inspections/sunbeam-products-inc/80662f75-1d5f-46af-b477-f7a18ec35995)

Company: https://www.keypedia.com/companies/sunbeam-products-inc/28411e97-2684-4185-8f20-75c67fbf77a1

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7