# Kellanova - Inspection Records

Source: https://www.globalkeysolutions.net/companies/kellanova/d58d97a6-e9a8-43ff-8ddd-1b6c0fdddb96

> Inspection records and compliance data for Kellanova in Cary, North Carolina. Access full analysis and detailed observations.

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## Details

- Name: Kellanova
- FEI Number: 1026111
- City: Cary
- State: North Carolina
- Country Name: United States
- Address Line 1: 1 Quality Ln
- Zip Code: 27513

## Related Documents

- [FDA Inspection 1228198 - Kellanova - 2024-01-18](https://www.globalkeysolutions.net/records/fda_inspections/kellanova/61ef7a48-8284-4cff-9b1b-564c3a274a19) — classification: No Action Indicated (NAI), source: FDA, date: January 18, 2024
- [FDA Inspection 1069246 - Kellanova - 2018-09-28](https://www.globalkeysolutions.net/records/fda_inspections/kellanova/d6445964-93b6-4bc1-b584-9b2e5c569b39) — classification: No Action Indicated (NAI), source: FDA, date: September 28, 2018
- [FDA Inspection 1013847 - Kellanova - 2017-04-24](https://www.globalkeysolutions.net/records/fda_inspections/kellanova/7a9d0a88-03e4-400f-a61c-0b8285d28bbb) — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2017
- [FDA Inspection 649663 - Kellanova - 2010-01-29](https://www.globalkeysolutions.net/records/fda_inspections/kellanova/a7ca75a2-2d68-4e16-9210-2c840f60bca7) — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2010
- [FDA Inspection 649663 - Kellanova - 2010-01-29](https://www.globalkeysolutions.net/records/fda_inspections/kellanova/62eaa8e5-b84f-44dc-8b43-d5cf0a614a8d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 29, 2010
- [FDA Inspection 649663 - Kellanova - 2010-01-29](https://www.globalkeysolutions.net/records/fda_inspections/kellanova/fb29f342-14e6-411e-b173-4f97aecd75f4) — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2010
- [CONSUMER_COMPLAINT_RECORD - Kellanova - 2009-02-03](https://www.globalkeysolutions.net/records/consumer_complaint_record/kellanova/1b29192d-d6e7-4f5e-be35-48738c269ac1) — source: FDA, date: February 3, 2009
- [CONSUMER_COMPLAINT_RECORD - Kellanova - 2009-01-30](https://www.globalkeysolutions.net/records/consumer_complaint_record/kellanova/418bfabc-550b-4822-bf97-6253b76d6d84) — source: FDA, date: January 30, 2009
- [CONSUMER_COMPLAINT_RECORD - Kellanova - 2009-01-28](https://www.globalkeysolutions.net/records/consumer_complaint_record/kellanova/f4089a21-7bfd-46c6-93f6-19a73c7e7825) — source: FDA, date: January 28, 2009
- [CONSUMER_COMPLAINT_RECORD - Kellanova - 2009-01-27](https://www.globalkeysolutions.net/records/consumer_complaint_record/kellanova/84b9c4e2-9c91-45ec-bb1e-c4a8162faa42) — source: FDA, date: January 27, 2009
- [CONSUMER_COMPLAINT_RECORD - Kellanova - 2009-01-24](https://www.globalkeysolutions.net/records/consumer_complaint_record/kellanova/69305ea1-ff72-4590-9859-ed457465e21e) — source: FDA, date: January 24, 2009
- [FDA Inspection 557431 - Kellanova - 2009-01-16](https://www.globalkeysolutions.net/records/fda_inspections/kellanova/dda927e7-a0b8-49e3-94bc-eb34f6602f3f) — classification: No Action Indicated (NAI), source: FDA, date: January 16, 2009

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