# Intermex Products USA, Ltd - Inspection Records

Source: https://www.keypedia.com/companies/intermex-products-usa-ltd/15cb8213-a1e0-4d81-a88d-5e3cd85c423e

> Inspection records and compliance data for Intermex Products USA, Ltd in Grand Prairie, Texas. Access full analysis and detailed observations.

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## Details

- Name: Intermex Products USA, Ltd
- FEI Number: 1640978
- City: Grand Prairie
- State: Texas
- Country Name: United States
- Address Line 1: 1375 Avenue S, Suite 300
- Zip Code: 75050

## Related Documents

- [FDA Inspection 1310136 - Intermex Products USA, Ltd - 2026-03-11](https://www.keypedia.com/records/fda_inspections/intermex-products-usa-ltd/05a4fe4e-1bb7-41f1-b757-bc56432976c4) — source: FDA, date: March 11, 2026
- [FDA Inspection 1310136 - Intermex Products USA, Ltd - 2026-03-11](https://www.keypedia.com/records/fda_inspections/intermex-products-usa-ltd/a1c30672-feaa-4cf5-8d17-a54c0c5731d9) — classification: No Action Indicated (NAI), source: FDA, date: March 11, 2026
- [FDA Inspection 1164967 - Intermex Products USA, Ltd - 2022-02-22](https://www.keypedia.com/records/fda_inspections/intermex-products-usa-ltd/cc4e1546-11ef-4e07-8aec-55dea9a0a454) — classification: No Action Indicated (NAI), source: FDA, date: February 22, 2022
- [FDA Inspection 1090146 - Intermex Products USA, Ltd - 2019-05-08](https://www.keypedia.com/records/fda_inspections/intermex-products-usa-ltd/00d03c9f-7d93-4ecf-a6ea-937b2b8ebc99) — classification: No Action Indicated (NAI), source: FDA, date: May 8, 2019
- [FDA Inspection 966881 - Intermex Products USA, Ltd - 2016-04-01](https://www.keypedia.com/records/fda_inspections/intermex-products-usa-ltd/4c2604f0-661d-472c-8125-8adb178dedd2) — classification: No Action Indicated (NAI), source: FDA, date: April 1, 2016
- [FDA Inspection 966881 - Intermex Products USA, Ltd - 2016-04-01](https://www.keypedia.com/records/fda_inspections/intermex-products-usa-ltd/c724e8da-9e9a-4e4e-aeb3-eb4023dc8de2) — classification: No Action Indicated (NAI), source: FDA, date: April 1, 2016
- [FDA Inspection 831102 - Intermex Products USA, Ltd - 2013-05-03](https://www.keypedia.com/records/fda_inspections/intermex-products-usa-ltd/470291cb-3848-4ec2-a075-fe6c301da49f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 3, 2013
- [FDA Inspection 831102 - Intermex Products USA, Ltd - 2013-05-03](https://www.keypedia.com/records/fda_inspections/intermex-products-usa-ltd/8a454951-e15e-479b-899f-51743b82481b) — classification: No Action Indicated (NAI), source: FDA, date: May 3, 2013
- [FDA Inspection 545828 - Intermex Products USA, Ltd - 2008-10-16](https://www.keypedia.com/records/fda_inspections/intermex-products-usa-ltd/9198b6fb-b2fe-4c6d-bebd-cb762401b9fb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 16, 2008
- [FDA Inspection 545828 - Intermex Products USA, Ltd - 2008-10-16](https://www.keypedia.com/records/fda_inspections/intermex-products-usa-ltd/5ff28947-c620-4f4e-a3d2-b4d47a7cc361) — classification: No Action Indicated (NAI), source: FDA, date: October 16, 2008

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