# Ridley USA Inc. - Inspection Records

Source: https://www.keypedia.com/companies/ridley-usa-inc/a63faf51-8fd6-4204-8965-938f1b40faa2

> Inspection records and compliance data for Ridley USA Inc. in Flemingsburg, Kentucky. Access full analysis and detailed observations.

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## Details

- Name: Ridley USA Inc.
- FEI Number: 3002816388
- City: Flemingsburg
- State: Kentucky
- Country Name: United States
- Address Line 1: 334 Industrial Park Dr
- Zip Code: 41041

## Related Documents

- [FDA Inspection 1282753 - Ridley USA Inc. - 2025-11-19](https://www.keypedia.com/records/fda_inspections/ridley-usa-inc/27c76e9c-b646-41e2-8088-a3d5a6286532) — source: FDA, date: November 19, 2025
- [FDA Inspection 1156900 - Ridley USA Inc. - 2021-10-22](https://www.keypedia.com/records/fda_inspections/ridley-usa-inc/b88e81ab-c8e8-4e12-a87d-bbdf99f31512) — classification: No Action Indicated (NAI), source: FDA, date: October 22, 2021
- [FDA Inspection 1127056 - Ridley USA Inc. - 2020-08-07](https://www.keypedia.com/records/fda_inspections/ridley-usa-inc/1f2f614d-b957-4e9a-a07d-68a70fd2e3b2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 7, 2020
- [FDA Inspection 1062710 - Ridley USA Inc. - 2018-05-25](https://www.keypedia.com/records/fda_inspections/ridley-usa-inc/cba7f136-ddd0-4861-9b91-4ed961db71f8) — classification: No Action Indicated (NAI), source: FDA, date: May 25, 2018
- [FDA Inspection 998784 - Ridley USA Inc. - 2017-01-19](https://www.keypedia.com/records/fda_inspections/ridley-usa-inc/27a1b421-cf75-42d3-922e-aec2e935a286) — classification: Official Action Indicated (OAI), source: FDA, date: January 19, 2017
- [FDA Inspection 759354 - Ridley USA Inc. - 2011-12-01](https://www.keypedia.com/records/fda_inspections/ridley-usa-inc/c86fae0c-e1eb-4ddc-bb12-e91bbf2aaae1) — classification: No Action Indicated (NAI), source: FDA, date: December 1, 2011
- [FDA Inspection 547247 - Ridley USA Inc. - 2008-10-21](https://www.keypedia.com/records/fda_inspections/ridley-usa-inc/68cac47a-6031-4034-892c-ded9934ce9fe) — classification: No Action Indicated (NAI), source: FDA, date: October 21, 2008

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