# Kraft Heinz - Inspection Records

Source: https://www.globalkeysolutions.net/companies/kraft-heinz/17137b3c-d36c-47ad-bbb3-022471f77b5f

> Inspection records and compliance data for Kraft Heinz in Muscatine, Iowa. Access full analysis and detailed observations.

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## Details

- Name: Kraft Heinz
- FEI Number: 1910119
- City: Muscatine
- State: Iowa
- Country Name: United States
- Address Line 1: 1357 Isett Ave
- Zip Code: 52761

## Related Documents

- [FDA Inspection 1231188 - Kraft Heinz - 2024-05-22](https://www.globalkeysolutions.net/records/fda_inspections/kraft-heinz/adf338c8-3639-4c0a-a8ea-f37d5dcc36cb) — classification: No Action Indicated (NAI), source: FDA, date: May 22, 2024
- [FDA Inspection 1160649 - Kraft Heinz - 2021-10-27](https://www.globalkeysolutions.net/records/fda_inspections/kraft-heinz/7b54310c-36be-46f5-b2db-dbb306ee8095) — classification: No Action Indicated (NAI), source: FDA, date: October 27, 2021
- [FDA Inspection 1031598 - Kraft Heinz - 2017-11-16](https://www.globalkeysolutions.net/records/fda_inspections/kraft-heinz/ff521fbc-e856-487d-99ad-233178c87a89) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 16, 2017
- [FDA Inspection 1031598 - Kraft Heinz - 2017-11-16](https://www.globalkeysolutions.net/records/fda_inspections/kraft-heinz/76556b31-68fb-4997-9fad-2e0dba1cf26e) — classification: No Action Indicated (NAI), source: FDA, date: November 16, 2017
- [FDA Inspection 909941 - Kraft Heinz - 2015-01-14](https://www.globalkeysolutions.net/records/fda_inspections/kraft-heinz/1696ec6e-3725-4536-bca1-01e12c62bc8c) — classification: No Action Indicated (NAI), source: FDA, date: January 14, 2015
- [FDA Inspection 842334 - Kraft Heinz - 2013-07-18](https://www.globalkeysolutions.net/records/fda_inspections/kraft-heinz/5e260610-2752-4363-aca6-ec807ba4c5bc) — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2013
- [FDA Inspection 744472 - Kraft Heinz - 2011-08-31](https://www.globalkeysolutions.net/records/fda_inspections/kraft-heinz/24f5e79c-efe1-409f-bcfc-cb6ffc7205fd) — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2011

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