# Hearthside Food Solutions, Michigan City, IN – FDA Inspections

Source: https://www.keypedia.com/companies/hearthside-food-solutions/e4804ea4-7ce0-4d38-9f0e-1f1c1be1dcd3

> Inspection records and compliance data for Hearthside Food Solutions in Michigan City, Indiana. 6 FDA inspections on record, 1 Form 483, last inspected August 04, 2023.

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## Details

- Name: Hearthside Food Solutions
- FEI Number: 1824241
- Address Line 1: 502 W US Highway 20
- City: Michigan City
- State: Indiana
- Zip Code: 46360
- Country Name: United States
- Address: 502 W US Highway 20, Michigan City, Indiana 46360, United States
- Country: United States

## Related Documents

- [FDA Inspection 1215104 - Hearthside Food Solutions - 2023-08-04](https://www.keypedia.com/records/fda_inspections/hearthside-food-solutions/6994eecd-ef7e-41a6-b93e-0ffa0ff23213) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 4, 2023
- FDA Inspection 1215104 - Hearthside Food Solutions - 2023-08-04 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 4, 2023
- FDA Inspection 1156790 - Hearthside Food Solutions - 2021-11-16 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 16, 2021
- FDA Inspection 1156790 - Hearthside Food Solutions - 2021-11-16 — classification: No Action Indicated (NAI), source: FDA, date: November 16, 2021
- FDA Inspection 1048159 - Hearthside Food Solutions - 2018-03-26 — classification: No Action Indicated (NAI), source: FDA, date: March 26, 2018
- FDA Inspection 1048159 - Hearthside Food Solutions - 2018-03-26 — classification: No Action Indicated (NAI), source: FDA, date: March 26, 2018
- FDA Inspection 955864 - Hearthside Food Solutions - 2015-12-21 — classification: No Action Indicated (NAI), source: FDA, date: December 21, 2015
- FDA Inspection 919192 - Hearthside Food Solutions - 2015-03-24 — classification: No Action Indicated (NAI), source: FDA, date: March 24, 2015
- FDA Inspection 727577 - Hearthside Food Solutions - 2011-05-26 — classification: No Action Indicated (NAI), source: FDA, date: May 26, 2011

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