FDA Inspection
Newell Brands, Inc.Newell Brands, Inc. – FDA Inspection, Sep 30, 2009
Record Details
This FDA Inspection record concerns Newell Brands, Inc., with an inspection on September 30, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Newell Brands, Inc.
- Inspection Date
- September 30, 2009
- Product Type
- Devices
View Company Profile
ID · 84e3aa6f-989f-43ab-8f8e-e48f75c99d62
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 614933
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 820.20(c)Management review participants
- 21 CFR 820.20(b)(2)Training
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
- 21 CFR 820.22Quality Audit/Reaudit - documentation
- 21 CFR 820.100(b)Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Newell Brands, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 18, 2026 | NAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
| November 3, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 26, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Newell Brands, Inc.
- FDA Inspection 1304546 - 2026-02-18
- FDA Inspection 991572 - 2016-11-03
- FDA Inspection 792966 - 2012-07-26
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