# Hearthside Food Solutions LLC, Woodridge, IL – FDA Inspections

Source: https://www.keypedia.com/companies/hearthside-food-solutions-llc/5e564e2f-264c-40a7-bde8-0cbeb0d54881

> Inspection records and compliance data for Hearthside Food Solutions LLC in Woodridge, Illinois. 7 FDA inspections on record, last inspected August 12, 2021.

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## Details

- Name: Hearthside Food Solutions LLC
- FEI Number: 1000139833
- Address Line 1: 10350 Argonne Dr Ste 200-400
- City: Woodridge
- State: Illinois
- Zip Code: 60517
- Country Name: United States
- Address: 10350 Argonne Dr Ste 200-400, Woodridge, Illinois 60517, United States
- Country: United States

## Related Documents

- FDA Inspection 1151718 - Hearthside Food Solutions LLC - 2021-08-12 — classification: No Action Indicated (NAI), source: FDA, date: August 12, 2021
- FDA Inspection 1151718 - Hearthside Food Solutions LLC - 2021-08-12 — classification: No Action Indicated (NAI), source: FDA, date: August 12, 2021
- FDA Inspection 1019514 - Hearthside Food Solutions LLC - 2017-05-02 — classification: No Action Indicated (NAI), source: FDA, date: May 2, 2017
- FDA Inspection 1019514 - Hearthside Food Solutions LLC - 2017-05-02 — classification: No Action Indicated (NAI), source: FDA, date: May 2, 2017
- FDA Inspection 872155 - Hearthside Food Solutions LLC - 2014-03-05 — classification: No Action Indicated (NAI), source: FDA, date: March 5, 2014
- FDA Inspection 772970 - Hearthside Food Solutions LLC - 2012-03-19 — classification: No Action Indicated (NAI), source: FDA, date: March 19, 2012
- [FDA Inspection 719030 - Hearthside Food Solutions LLC - 2011-04-12](https://www.keypedia.com/records/fda_inspections/hearthside-food-solutions-llc/759a072e-3ec8-456e-b737-e56194239b20) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 12, 2011
- FDA Inspection 666848 - Hearthside Food Solutions LLC - 2010-06-15 — classification: No Action Indicated (NAI), source: FDA, date: June 15, 2010
- FDA Inspection 603871 - Hearthside Food Solutions LLC - 2009-08-13 — classification: No Action Indicated (NAI), source: FDA, date: August 13, 2009

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