# FDA Inspection 984399 - Sunbeam Products Inc. - July 08, 2016

Source: https://www.keypedia.com/records/fda_inspections/sunbeam-products-inc/7c57f32e-bec8-474e-aa3c-89e95f2721fa
Source feed: FDA_Inspections

> FDA Inspection 984399 for Sunbeam Products Inc. on July 08, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 984399
- Company Name: Sunbeam Products Inc.
- Inspection Date: 2016-07-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 984399 - 2016-07-08](https://www.keypedia.com/records/fda_inspections/sunbeam-products-inc/440f0aed-3bf6-4510-abaf-2c731cd6b84f)
- [FDA Inspection 869263 - 2014-02-28](https://www.keypedia.com/records/fda_inspections/sunbeam-products-inc/6d4a12d9-e290-4421-9307-5b36b73cac1a)
- [FDA Inspection 869263 - 2014-02-28](https://www.keypedia.com/records/fda_inspections/sunbeam-products-inc/d8fcdf59-1364-4b14-8be9-9bc188bb401c)
- [FDA Inspection 830448 - 2013-05-03](https://www.keypedia.com/records/fda_inspections/sunbeam-products-inc/b9a54256-11fc-4d8d-8bc2-f5fcb2efee77)
- [FDA Inspection 830448 - 2013-05-03](https://www.keypedia.com/records/fda_inspections/sunbeam-products-inc/7cd9a49a-f444-406d-8f33-fc0ccceb293a)

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