# Cheesecake Factory Inc, The - Inspection Records

Source: https://www.globalkeysolutions.net/companies/cheesecake-factory-inc-the/6c23ba66-1e39-4a59-b87d-7a010746481d

> Inspection records and compliance data for Cheesecake Factory Inc, The in Calabasas, California. Access full analysis and detailed observations.

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## Details

- Name: Cheesecake Factory Inc, The
- FEI Number: 3000181722
- City: Calabasas
- State: California
- Country Name: United States
- Address Line 1: 26950 Agoura Rd
- Zip Code: 91301

## Related Documents

- [483 - Cheesecake Factory Inc, The - 2025-10-22](https://www.globalkeysolutions.net/records/483/cheesecake-factory-inc-the/4955df2e-4b26-4dbe-83c8-cb77a50d189d) — source: FDA, date: October 22, 2025
- [FDA Inspection 1278888 - Cheesecake Factory Inc, The - 2025-10-22](https://www.globalkeysolutions.net/records/fda_inspections/cheesecake-factory-inc-the/65ef0481-43b0-4dcb-98cd-641d74dcffcd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 22, 2025
- [FDA Inspection 1278888 - Cheesecake Factory Inc, The - 2025-10-22](https://www.globalkeysolutions.net/records/fda_inspections/cheesecake-factory-inc-the/59ccf61f-9a2e-425b-af77-1b695e7b4985) — classification: No Action Indicated (NAI), source: FDA, date: October 22, 2025
- [FDA Inspection 1278888 - Cheesecake Factory Inc, The - 2025-10-22](https://www.globalkeysolutions.net/records/fda_inspections/cheesecake-factory-inc-the/4cb5c717-9931-4645-84da-b42c25830d81) — classification: No Action Indicated (NAI), source: FDA, date: October 22, 2025
- [FDA Inspection 1143081 - Cheesecake Factory Inc, The - 2021-05-27](https://www.globalkeysolutions.net/records/fda_inspections/cheesecake-factory-inc-the/219844f7-fdec-43cc-ad8c-a50179e9bbc8) — classification: No Action Indicated (NAI), source: FDA, date: May 27, 2021
- [FDA Inspection 711891 - Cheesecake Factory Inc, The - 2011-03-03](https://www.globalkeysolutions.net/records/fda_inspections/cheesecake-factory-inc-the/e22361da-da7b-45cd-957b-1dcf59a1b2b4) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2011

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