# Sunbeam Products Inc. – FDA Inspection, May 3, 2013

Source: https://www.keypedia.com/records/fda_inspections/sunbeam-products-inc/b9a54256-11fc-4d8d-8bc2-f5fcb2efee77
Source feed: FDA_Inspections

> FDA inspection 830448 of Sunbeam Products Inc., May 03, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 830448
- Company Name: Sunbeam Products Inc.
- Inspection Date: 2013-05-03
- 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 984399 - 2016-07-08
- [FDA Inspection 869263 - 2014-02-28](https://www.keypedia.com/records/fda_inspections/sunbeam-products-inc/d8fcdf59-1364-4b14-8be9-9bc188bb401c)

Company: https://www.keypedia.com/companies/sunbeam-products-inc/6cce49cb-bb15-49c3-be86-d389a13f6c0a

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