# Kellanova/Kellogg Co Inc, Zanesville, OH – FDA Inspections

Source: https://www.keypedia.com/companies/kellanovakellogg-co-inc/1c62cb07-abe4-42da-b5eb-865a2ea0e7ed

> Inspection records and compliance data for Kellanova/Kellogg Co Inc in Zanesville, Ohio. 4 FDA inspections on record, last inspected May 10, 2017.

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## Details

- Name: Kellanova/Kellogg Co Inc
- FEI Number: 1000160096
- Address Line 1: 1675 Fairview Rd
- City: Zanesville
- State: Ohio
- Zip Code: 43701
- Country Name: United States
- Address: 1675 Fairview Rd, Zanesville, Ohio 43701, United States
- Country: United States

## Related Documents

- FDA Inspection 1011638 - Kellanova/Kellogg Co Inc - 2017-05-10 — classification: No Action Indicated (NAI), source: FDA, date: May 10, 2017
- FDA Inspection 954071 - Kellanova/Kellogg Co Inc - 2015-11-24 — classification: No Action Indicated (NAI), source: FDA, date: November 24, 2015
- FDA Inspection 954071 - Kellanova/Kellogg Co Inc - 2015-11-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 24, 2015
- FDA Inspection 954071 - Kellanova/Kellogg Co Inc - 2015-11-24 — classification: No Action Indicated (NAI), source: FDA, date: November 24, 2015
- FDA Inspection 954071 - Kellanova/Kellogg Co Inc - 2015-11-24 — classification: No Action Indicated (NAI), source: FDA, date: November 24, 2015
- FDA Inspection 654584 - Kellanova/Kellogg Co Inc - 2010-03-11 — classification: No Action Indicated (NAI), source: FDA, date: March 11, 2010
- FDA Inspection 637710 - Kellanova/Kellogg Co Inc - 2010-01-12 — classification: No Action Indicated (NAI), source: FDA, date: January 12, 2010
- FDA Inspection 637710 - Kellanova/Kellogg Co Inc - 2010-01-12 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 12, 2010
- FDA Inspection 637710 - Kellanova/Kellogg Co Inc - 2010-01-12 — classification: No Action Indicated (NAI), source: FDA, date: January 12, 2010
- FDA Inspection 637710 - Kellanova/Kellogg Co Inc - 2010-01-12 — classification: No Action Indicated (NAI), source: FDA, date: January 12, 2010

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