# McCarthy Spice & Blends Company - Inspection Records

Source: https://www.keypedia.com/companies/mccarthy-spice-blends-company/f49aaddd-39bc-45d7-bfee-5da7372bb0a9

> Inspection records and compliance data for McCarthy Spice & Blends Company in Saint Louis, Missouri. Access full analysis and detailed observations.

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## Details

- Name: McCarthy Spice & Blends Company
- FEI Number: 3000203082
- City: Saint Louis
- State: Missouri
- Country Name: United States
- Address Line 1: 8501 Delport Dr
- Zip Code: 63114

## Related Documents

- [FDA Inspection 1261394 - McCarthy Spice & Blends Company - 2025-02-13](https://www.keypedia.com/records/fda_inspections/mccarthy-spice-blends-company/b61a1e3b-8289-42e9-8f43-c4ae008f9b17) — source: FDA, date: February 13, 2025
- [FDA Inspection 1206731 - McCarthy Spice & Blends Company - 2023-05-25](https://www.keypedia.com/records/fda_inspections/mccarthy-spice-blends-company/b32567c4-8201-4970-ba50-8b83f70b6067) — classification: No Action Indicated (NAI), source: FDA, date: May 25, 2023
- [FDA Inspection 1161526 - McCarthy Spice & Blends Company - 2021-12-15](https://www.keypedia.com/records/fda_inspections/mccarthy-spice-blends-company/6f0185bf-c895-4276-afea-bf7dac93f37e) — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2021
- [FDA Inspection 1161526 - McCarthy Spice & Blends Company - 2021-12-15](https://www.keypedia.com/records/fda_inspections/mccarthy-spice-blends-company/5b922b2a-9be1-4d10-81d5-ce26971884bd) — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2021
- [FDA Inspection 1040028 - McCarthy Spice & Blends Company - 2017-12-19](https://www.keypedia.com/records/fda_inspections/mccarthy-spice-blends-company/6db19dda-41f8-42ad-8199-f6aaf1ab94dc) — classification: No Action Indicated (NAI), source: FDA, date: December 19, 2017
- [FDA Inspection 1036788 - McCarthy Spice & Blends Company - 2017-10-31](https://www.keypedia.com/records/fda_inspections/mccarthy-spice-blends-company/b1941e73-431c-4f11-ace5-237e78257cb7) — classification: No Action Indicated (NAI), source: FDA, date: October 31, 2017

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