# American Italian Pasta Company - Inspection Records

Source: https://www.keypedia.com/companies/american-italian-pasta-company/e94a3832-d33d-4f4f-a181-307eae865338

> Inspection records and compliance data for American Italian Pasta Company in Saint Louis, Missouri. Access full analysis and detailed observations.

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## Details

- Name: American Italian Pasta Company
- FEI Number: 1940189
- City: Saint Louis
- State: Missouri
- Country Name: United States
- Address Line 1: 611 E Marceau St
- Zip Code: 63111

## Related Documents

- [FDA Inspection 1251700 - American Italian Pasta Company - 2025-04-30](https://www.keypedia.com/records/fda_inspections/american-italian-pasta-company/11714b80-f582-43df-a428-7cfbd3094d72) — source: FDA, date: April 30, 2025
- [FDA Inspection 1251700 - American Italian Pasta Company - 2025-04-30](https://www.keypedia.com/records/fda_inspections/american-italian-pasta-company/674f03bc-9665-4039-89c9-753a69f3e696) — classification: No Action Indicated (NAI), source: FDA, date: April 30, 2025
- [FDA Inspection 1195241 - American Italian Pasta Company - 2023-01-12](https://www.keypedia.com/records/fda_inspections/american-italian-pasta-company/07652143-bfcd-4f03-a6e6-bf0b2975d2c1) — classification: No Action Indicated (NAI), source: FDA, date: January 12, 2023
- [FDA Inspection 1166432 - American Italian Pasta Company - 2022-03-29](https://www.keypedia.com/records/fda_inspections/american-italian-pasta-company/4055defa-b414-4e23-8ab4-b0882901026c) — classification: No Action Indicated (NAI), source: FDA, date: March 29, 2022
- [FDA Inspection 1028310 - American Italian Pasta Company - 2017-06-23](https://www.keypedia.com/records/fda_inspections/american-italian-pasta-company/63d327ca-2d01-4790-9907-8eb7f7b4bcf1) — classification: No Action Indicated (NAI), source: FDA, date: June 23, 2017
- [FDA Inspection 981006 - American Italian Pasta Company - 2016-07-12](https://www.keypedia.com/records/fda_inspections/american-italian-pasta-company/c2af5480-d5ed-4d71-8974-efa42ee4c41b) — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2016

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