# Cargill Kitchen Solutions, Inc - Inspection Records

Source: https://www.keypedia.com/companies/cargill-kitchen-solutions-inc/cd0feb09-4d12-4bd5-983d-3d678a676483

> Inspection records and compliance data for Cargill Kitchen Solutions, Inc in Monticello, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Cargill Kitchen Solutions, Inc
- FEI Number: 2128184
- City: Monticello
- State: Minnesota
- Country Name: United States
- Address Line 1: 206 W 4th St
- Zip Code: 55362

## Related Documents

- [FDA Inspection 1254841 - Cargill Kitchen Solutions, Inc - 2024-11-13](https://www.keypedia.com/records/fda_inspections/cargill-kitchen-solutions-inc/a92b8b1f-b3c2-484b-8724-236441f6f285) — source: FDA, date: November 13, 2024
- [FDA Inspection 1254841 - Cargill Kitchen Solutions, Inc - 2024-11-13](https://www.keypedia.com/records/fda_inspections/cargill-kitchen-solutions-inc/2564d11d-0e31-4998-b55b-5e6ecad36c41) — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2024
- [FDA Inspection 1166393 - Cargill Kitchen Solutions, Inc - 2022-03-10](https://www.keypedia.com/records/fda_inspections/cargill-kitchen-solutions-inc/1f818a81-7f73-4728-87d0-1baaf5d631c0) — classification: No Action Indicated (NAI), source: FDA, date: March 10, 2022
- [FDA Inspection 769485 - Cargill Kitchen Solutions, Inc - 2012-02-24](https://www.keypedia.com/records/fda_inspections/cargill-kitchen-solutions-inc/d10c00ab-cf9c-4ff5-b541-1e33b64cbfb5) — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2012
- [FDA Inspection 682620 - Cargill Kitchen Solutions, Inc - 2010-09-21](https://www.keypedia.com/records/fda_inspections/cargill-kitchen-solutions-inc/6c0b24ca-5229-43a3-82bd-e1939d0459ca) — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2010
- [FDA Inspection 580995 - Cargill Kitchen Solutions, Inc - 2009-05-04](https://www.keypedia.com/records/fda_inspections/cargill-kitchen-solutions-inc/540b2708-be37-4d30-8ce4-6731e9e922ac) — classification: No Action Indicated (NAI), source: FDA, date: May 4, 2009

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