# Ozark Empire Distributors, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/ozark-empire-distributors-inc/ac5ca724-157a-4e0c-a9f1-1f5652d4d0ce

> Inspection records and compliance data for Ozark Empire Distributors, Inc. in Rogers, Arkansas. Access full analysis and detailed observations.

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## Details

- Name: Ozark Empire Distributors, Inc.
- FEI Number: 2315117
- City: Rogers
- State: Arkansas
- Country Name: United States
- Address Line 1: 2301 S 1st St
- Zip Code: 72758

## Related Documents

- [FDA Inspection 1267199 - Ozark Empire Distributors, Inc. - 2025-04-07](https://www.keypedia.com/records/fda_inspections/ozark-empire-distributors-inc/384ad4c3-8fc1-4ee1-b541-26b5f720e7a8) — source: FDA, date: April 7, 2025
- [FDA Inspection 1267199 - Ozark Empire Distributors, Inc. - 2025-04-07](https://www.keypedia.com/records/fda_inspections/ozark-empire-distributors-inc/3f57ed7a-f5f0-468c-a324-714babb46e7c) — classification: No Action Indicated (NAI), source: FDA, date: April 7, 2025
- [FDA Inspection 1156011 - Ozark Empire Distributors, Inc. - 2021-11-03](https://www.keypedia.com/records/fda_inspections/ozark-empire-distributors-inc/178f4646-b34b-44d0-a19f-fbd612148f9c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 3, 2021
- [FDA Inspection 1056481 - Ozark Empire Distributors, Inc. - 2018-06-04](https://www.keypedia.com/records/fda_inspections/ozark-empire-distributors-inc/2fd24047-9cf2-4c88-a140-f128beaa1357) — classification: No Action Indicated (NAI), source: FDA, date: June 4, 2018
- [FDA Inspection 900618 - Ozark Empire Distributors, Inc. - 2014-10-20](https://www.keypedia.com/records/fda_inspections/ozark-empire-distributors-inc/c0f7c589-1c80-4f57-bba2-62fa3867f5d1) — classification: No Action Indicated (NAI), source: FDA, date: October 20, 2014
- [FDA Inspection 793520 - Ozark Empire Distributors, Inc. - 2012-08-02](https://www.keypedia.com/records/fda_inspections/ozark-empire-distributors-inc/4257fa54-1561-4ff7-a79f-d5fce78b2e5f) — classification: No Action Indicated (NAI), source: FDA, date: August 2, 2012

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