# Cookie Jar Collection, Inc - Inspection Records

Source: https://www.keypedia.com/companies/cookie-jar-collection-inc/e27cd1b8-4843-4a7b-81e6-0769ebe49fe5

> Inspection records and compliance data for Cookie Jar Collection, Inc in Huntington Beach, California. Access full analysis and detailed observations.

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## Details

- Name: Cookie Jar Collection, Inc
- FEI Number: 3004493907
- City: Huntington Beach
- State: California
- Country Name: United States
- Address Line 1: 17682 Sampson Ln
- Zip Code: 92647

## Related Documents

- [FDA Inspection 1219765 - Cookie Jar Collection, Inc - 2023-10-06](https://www.keypedia.com/records/fda_inspections/cookie-jar-collection-inc/5485cccc-fbef-47fa-822c-28d13ffbd5cf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 6, 2023
- [FDA Inspection 1219765 - Cookie Jar Collection, Inc - 2023-10-06](https://www.keypedia.com/records/fda_inspections/cookie-jar-collection-inc/1f61d776-9a9a-4598-8dae-95e31d98d3d4) — classification: No Action Indicated (NAI), source: FDA, date: October 6, 2023
- [FDA Inspection 1139715 - Cookie Jar Collection, Inc - 2021-04-08](https://www.keypedia.com/records/fda_inspections/cookie-jar-collection-inc/4cee5080-2e95-409a-99ab-46e4dcdad15a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 8, 2021
- [FDA Inspection 1004933 - Cookie Jar Collection, Inc - 2017-02-15](https://www.keypedia.com/records/fda_inspections/cookie-jar-collection-inc/d0ece52e-eaff-4334-b9a6-2c44e3f06280) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 15, 2017
- [FDA Inspection 702016 - Cookie Jar Collection, Inc - 2010-10-19](https://www.keypedia.com/records/fda_inspections/cookie-jar-collection-inc/cc1ff0a0-7172-4c5b-8f7b-c1842490139a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 19, 2010
- [FDA Inspection 702016 - Cookie Jar Collection, Inc - 2010-10-19](https://www.keypedia.com/records/fda_inspections/cookie-jar-collection-inc/8bf39e83-be58-4e83-a422-fe5bd735491c) — classification: No Action Indicated (NAI), source: FDA, date: October 19, 2010

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