# Newell Brands, Inc. – FDA Inspection, Sep 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/newell-brands-inc/84e3aa6f-989f-43ab-8f8e-e48f75c99d62
Source feed: FDA_Inspections

> FDA inspection 614933 of Newell Brands, Inc., September 30, 2009. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 614933
- Company Name: Newell Brands, Inc.
- Inspection Date: 2009-09-30
- 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: 5

## Related Documents

- FDA Inspection 1304546 - 2026-02-18
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- FDA Inspection 792966 - 2012-07-26

Company: https://www.keypedia.com/companies/newell-brands-inc/f6f13555-10dc-4dbf-af5a-e6c1098a8146

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