FDA Inspection
Sunbeam Products, Inc.Sunbeam Products, Inc. – FDA Inspection, Jun 28, 2013
Record Details
This FDA Inspection record concerns Sunbeam Products, Inc., with an inspection on June 28, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Sunbeam Products, Inc.
- Inspection Date
- June 28, 2013
- Product Type
- Devices
View Company Profile
ID · 31c929ab-d35c-48ed-a952-17399aca081a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 839700
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(b)Documentation
- 21 CFR 820.198(e)Records of complaint investigation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Sunbeam Products, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 23, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 19, 2015 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 3, 2012 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 30, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Sunbeam Products, Inc.
- FDA Inspection 1067545 - 2018-08-23
- FDA Inspection 933679 - 2015-06-19
- FDA Inspection 793902 - 2012-08-03
- FDA Inspection 625873 - 2009-10-30
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