# American Licorice Company, Union City, CA – FDA Inspections

Source: https://www.keypedia.com/companies/american-licorice-company/21e2cb36-9154-4014-876b-3f1c604a0ee4

> Inspection records and compliance data for American Licorice Company in Union City, California. 6 FDA inspections on record, last inspected May 29, 2025.

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## Details

- Name: American Licorice Company
- FEI Number: 2910055
- Address Line 1: 2477 Liston Way
- City: Union City
- State: California
- Zip Code: 94587
- Country Name: United States
- Address: 2477 Liston Way, Union City, California 94587, United States
- Country: United States

## Related Documents

- FDA Inspection 1261980 - American Licorice Company - 2025-05-29 — classification: No Action Indicated (NAI), source: FDA, date: May 29, 2025
- FDA Inspection 1151650 - American Licorice Company - 2021-09-09 — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2021
- FDA Inspection 1151650 - American Licorice Company - 2021-09-09 — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2021
- FDA Inspection 1060732 - American Licorice Company - 2018-06-18 — classification: No Action Indicated (NAI), source: FDA, date: June 18, 2018
- FDA Inspection 878194 - American Licorice Company - 2014-05-06 — classification: No Action Indicated (NAI), source: FDA, date: May 6, 2014
- FDA Inspection 878194 - American Licorice Company - 2014-05-06 — classification: No Action Indicated (NAI), source: FDA, date: May 6, 2014
- FDA Inspection 802607 - American Licorice Company - 2012-10-11 — classification: No Action Indicated (NAI), source: FDA, date: October 11, 2012
- FDA Inspection 802607 - American Licorice Company - 2012-10-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 11, 2012
- FDA Inspection 705408 - American Licorice Company - 2011-01-13 — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2011
- FDA Inspection 705408 - American Licorice Company - 2011-01-13 — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2011

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