# Lyons Magnus East, LLC, Walton, KY – FDA Inspections

Source: https://www.keypedia.com/companies/lyons-magnus-east-llc/5fac9481-63be-4336-bc55-f08020b12973

> Inspection records and compliance data for Lyons Magnus East, LLC in Walton, Kentucky. 10 FDA inspections on record, last inspected August 20, 2026.

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## Details

- Name: Lyons Magnus East, LLC
- FEI Number: 1034904
- Address Line 1: 95 Richwood Rd
- City: Walton
- State: Kentucky
- Zip Code: 41094
- Country Name: United States
- Address: 95 Richwood Rd, Walton, Kentucky 41094, United States
- Country: United States

## Related Documents

- FDA Inspection 1330380 - Lyons Magnus East, LLC - 2026-08-20 — classification: No Action Indicated (NAI), source: FDA, date: August 20, 2026
- FDA Inspection 1330380 - Lyons Magnus East, LLC - 2026-08-20 — classification: No Action Indicated (NAI), source: FDA, date: August 20, 2026
- [FDA Inspection 1300760 - Lyons Magnus East, LLC - 2026-01-15](https://www.keypedia.com/records/fda_inspections/lyons-magnus-east-llc/c63670f3-8931-4666-9c15-5ac720703428) — source: FDA, date: January 15, 2026
- FDA Inspection 1300760 - Lyons Magnus East, LLC - 2026-01-15 — classification: No Action Indicated (NAI), source: FDA, date: January 15, 2026
- FDA Inspection 1300760 - Lyons Magnus East, LLC - 2026-01-15 — classification: No Action Indicated (NAI), source: FDA, date: January 15, 2026
- FDA Inspection 1278204 - Lyons Magnus East, LLC - 2025-07-31 — source: FDA, date: July 31, 2025
- FDA Inspection 1198657 - Lyons Magnus East, LLC - 2023-02-22 — source: FDA, date: February 22, 2023
- FDA Inspection 1106243 - Lyons Magnus East, LLC - 2019-10-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 8, 2019
- FDA Inspection 1045493 - Lyons Magnus East, LLC - 2018-03-07 — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2018
- [FDA Inspection 1045493 - Lyons Magnus East, LLC - 2018-03-07](https://www.keypedia.com/records/fda_inspections/lyons-magnus-east-llc/fd75ff3e-c011-4c16-8f93-e41d1e16b2f3) — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2018

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