# Egbert OK Livestock, Botkins, OH – FDA Inspections

Source: https://www.keypedia.com/companies/egbert-ok-livestock/31c94917-ed03-48ce-9262-9bbb028f9714

> Inspection records and compliance data for Egbert OK Livestock in Botkins, Ohio. 9 FDA inspections on record (1 OAI), last inspected June 01, 2026.

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## Details

- Name: Egbert OK Livestock
- FEI Number: 1526470
- Address Line 1: 10341 Botkins Rd
- City: Botkins
- State: Ohio
- Zip Code: 45306
- Country Name: United States
- Address: 10341 Botkins Rd, Botkins, Ohio 45306, United States
- Country: United States

## Related Documents

- FDA Inspection 1320212 - Egbert OK Livestock - 2026-06-01 — source: FDA, date: June 1, 2026
- FDA Inspection 1269034 - Egbert OK Livestock - 2025-04-24 — source: FDA, date: April 24, 2025
- [FDA Inspection 1269034 - Egbert OK Livestock - 2025-04-24](https://www.keypedia.com/records/fda_inspections/egbert-ok-livestock/85e49e55-1a35-4b13-9b1a-8bcc56bb9175) — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2025
- FDA Inspection 1044821 - Egbert OK Livestock - 2018-02-16 — classification: No Action Indicated (NAI), source: FDA, date: February 16, 2018
- FDA Inspection 912580 - Egbert OK Livestock - 2015-01-14 — classification: No Action Indicated (NAI), source: FDA, date: January 14, 2015
- FDA Inspection 887936 - Egbert OK Livestock - 2014-06-20 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2014
- FDA Inspection 836257 - Egbert OK Livestock - 2013-06-11 — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2013
- [FDA Inspection 677536 - Egbert OK Livestock - 2010-09-23](https://www.keypedia.com/records/fda_inspections/egbert-ok-livestock/8f0774d4-09b5-41f2-ac6e-bc5d05cd5faf) — classification: Official Action Indicated (OAI), source: FDA, date: September 23, 2010
- FDA Inspection 587358 - Egbert OK Livestock - 2009-05-13 — classification: No Action Indicated (NAI), source: FDA, date: May 13, 2009
- FDA Inspection 577324 - Egbert OK Livestock - 2009-03-24 — classification: No Action Indicated (NAI), source: FDA, date: March 24, 2009

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