# Catallia Mexican Foods, LLC - Inspection Records

Source: https://www.keypedia.com/companies/catallia-mexican-foods-llc/cacb3ab9-8678-4ae0-a4cc-a5ff18f55994

> Inspection records and compliance data for Catallia Mexican Foods, LLC in Eagan, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Catallia Mexican Foods, LLC
- FEI Number: 2000008176
- City: Eagan
- State: Minnesota
- Country Name: United States
- Address Line 1: 2965 Lone Oak Cir
- Zip Code: 55121

## Related Documents

- [FDA Inspection 1218718 - Catallia Mexican Foods, LLC - 2023-09-25](https://www.keypedia.com/records/fda_inspections/catallia-mexican-foods-llc/6481aa0a-c1a4-4fc4-8aac-5e540d5bb1a6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 25, 2023
- [FDA Inspection 1032105 - Catallia Mexican Foods, LLC - 2017-11-24](https://www.keypedia.com/records/fda_inspections/catallia-mexican-foods-llc/15694d5c-7cdd-4745-b2c5-2e620ab649b4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 24, 2017
- [FDA Inspection 991191 - Catallia Mexican Foods, LLC - 2016-10-28](https://www.keypedia.com/records/fda_inspections/catallia-mexican-foods-llc/99ffd776-9750-4541-b840-9137c919f298) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 28, 2016
- [FDA Inspection 856828 - Catallia Mexican Foods, LLC - 2013-11-14](https://www.keypedia.com/records/fda_inspections/catallia-mexican-foods-llc/0d13b02a-74cf-48af-9da8-8efa5b26888c) — classification: No Action Indicated (NAI), source: FDA, date: November 14, 2013
- [FDA Inspection 856828 - Catallia Mexican Foods, LLC - 2013-11-14](https://www.keypedia.com/records/fda_inspections/catallia-mexican-foods-llc/bfb70ebb-5b74-4cfc-b498-42c59029e3c5) — classification: No Action Indicated (NAI), source: FDA, date: November 14, 2013
- [FDA Inspection 718132 - Catallia Mexican Foods, LLC - 2011-04-05](https://www.keypedia.com/records/fda_inspections/catallia-mexican-foods-llc/00cb9d84-6de2-4fb7-8ec7-74de67e29bc6) — classification: No Action Indicated (NAI), source: FDA, date: April 5, 2011

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