# Miyoshi America, Inc - Inspection Records

Source: https://www.keypedia.com/companies/miyoshi-america-inc/b8b68045-2f79-4dab-a8b0-08e43de931cb

> Inspection records and compliance data for Miyoshi America, Inc in Dayville, Connecticut. Access full analysis and detailed observations.

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## Details

- Name: Miyoshi America, Inc
- FEI Number: 3009481791
- City: Dayville
- State: Connecticut
- Country Name: United States
- Address Line 1: 110 Louisa Viens Dr
- Zip Code: 06241

## Related Documents

- [FDA Inspection 1306728 - Miyoshi America, Inc - 2026-02-06](https://www.keypedia.com/records/fda_inspections/miyoshi-america-inc/ac1adf18-2faf-4a07-8280-d7e05f2e174a) — source: FDA, date: February 6, 2026
- [FDA Inspection 1306728 - Miyoshi America, Inc - 2026-02-06](https://www.keypedia.com/records/fda_inspections/miyoshi-america-inc/6d0a44e8-af00-4c02-9677-4d504f79134b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 6, 2026
- [483 - Miyoshi America, Inc - 2023-01-13](https://www.keypedia.com/records/483/miyoshi-america-inc/804d29f6-1061-4616-98b0-4c313616829d) — source: FDA, date: January 13, 2023
- [FDA Inspection 1198326 - Miyoshi America, Inc - 2023-01-13](https://www.keypedia.com/records/fda_inspections/miyoshi-america-inc/3da6d54d-300a-4547-9433-a29e7c20d217) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2023
- [483 - Miyoshi America, Inc - 2021-05-25](https://www.keypedia.com/records/483/miyoshi-america-inc/ca07a1a9-e443-43d4-ae69-8ffd6fadd238) — source: FDA, date: May 25, 2021
- [FDA Inspection 1144549 - Miyoshi America, Inc - 2021-05-25](https://www.keypedia.com/records/fda_inspections/miyoshi-america-inc/2a38b802-d721-4010-afa3-2e555ecdbfe0) — classification: Official Action Indicated (OAI), source: FDA, date: May 25, 2021
- [FDA Inspection 974319 - Miyoshi America, Inc - 2016-06-03](https://www.keypedia.com/records/fda_inspections/miyoshi-america-inc/27a49291-c83c-4b7f-9cc7-93eb36113c26) — classification: No Action Indicated (NAI), source: FDA, date: June 3, 2016
- [FDA Inspection 950532 - Miyoshi America, Inc - 2015-11-17](https://www.keypedia.com/records/fda_inspections/miyoshi-america-inc/a78288bc-1b47-476d-9325-c8bea15b76b5) — classification: No Action Indicated (NAI), source: FDA, date: November 17, 2015
- [FDA Inspection 737348 - Miyoshi America, Inc - 2011-07-20](https://www.keypedia.com/records/fda_inspections/miyoshi-america-inc/37d58ace-8951-4ef2-bb00-594b95adbcbc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 20, 2011

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