# Tyson Poultry, Inc, Springdale, AR – FDA Inspections

Source: https://www.keypedia.com/companies/tyson-poultry-inc/50b0f205-afa8-4b8e-bce0-b14e17efb39e

> Inspection records and compliance data for Tyson Poultry, Inc in Springdale, Arkansas. 10 FDA inspections on record, last inspected September 18, 2023.

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## Details

- Name: Tyson Poultry, Inc
- FEI Number: 2314954
- Address Line 1: 3801 Johnson Rd
- City: Springdale
- State: Arkansas
- Zip Code: 72762
- Country Name: United States
- Address: 3801 Johnson Rd, Springdale, Arkansas 72762, United States
- Country: United States

## Related Documents

- FDA Inspection 1219729 - Tyson Poultry, Inc - 2023-09-18 — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2023
- FDA Inspection 1069797 - Tyson Poultry, Inc - 2018-06-20 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2018
- FDA Inspection 958969 - Tyson Poultry, Inc - 2015-11-04 — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2015
- FDA Inspection 902376 - Tyson Poultry, Inc - 2014-10-29 — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2014
- [FDA Inspection 855974 - Tyson Poultry, Inc - 2013-11-22](https://www.keypedia.com/records/fda_inspections/tyson-poultry-inc/a6e63f6d-4098-4b3b-83bd-6e32b30ae4d9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 22, 2013
- FDA Inspection 821187 - Tyson Poultry, Inc - 2013-02-12 — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2013
- FDA Inspection 753780 - Tyson Poultry, Inc - 2011-11-04 — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2011
- FDA Inspection 696005 - Tyson Poultry, Inc - 2010-10-20 — classification: No Action Indicated (NAI), source: FDA, date: October 20, 2010
- FDA Inspection 642856 - Tyson Poultry, Inc - 2010-01-27 — classification: No Action Indicated (NAI), source: FDA, date: January 27, 2010
- FDA Inspection 557403 - Tyson Poultry, Inc - 2009-01-22 — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2009

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