# Biomat USA, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/biomat-usa-inc/88b3327f-0598-4bf4-a111-e892b5929f9e

> Inspection records and compliance data for Biomat USA, Inc. in El Paso, Texas. Access full analysis and detailed observations.

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## Details

- Name: Biomat USA, Inc.
- FEI Number: 1626579
- City: El Paso
- State: Texas
- Country Name: United States
- Address Line 1: 720 Texas Ave
- Zip Code: 79901

## Related Documents

- [FDA Inspection 1220702 - Biomat USA, Inc. - 2023-08-30](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/d2a10cf3-3250-4c0f-9e3e-d50466068aa3) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2023
- [FDA Inspection 1220702 - Biomat USA, Inc. - 2023-08-30](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/47376061-3b60-4533-bed9-2f62ee2ea73c) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2023
- [FDA Inspection 1028285 - Biomat USA, Inc. - 2017-09-14](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/c7037bb7-6b6f-4093-8fba-dc5df090468c) — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2017
- [FDA Inspection 938626 - Biomat USA, Inc. - 2015-07-22](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/4eb6fd3d-6017-4d9c-9538-c54802df8f50) — classification: No Action Indicated (NAI), source: FDA, date: July 22, 2015
- [FDA Inspection 865387 - Biomat USA, Inc. - 2014-01-30](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/28eb1dda-b25c-4415-a3e8-d780ea4acff0) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2014
- [FDA Inspection 762503 - Biomat USA, Inc. - 2012-01-11](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/a5a72430-4816-43bc-b94e-c1ac3215e498) — classification: No Action Indicated (NAI), source: FDA, date: January 11, 2012
- [FDA Inspection 627926 - Biomat USA, Inc. - 2009-11-13](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/a785de99-a1dd-44c4-9cff-8d42524a3d4c) — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2009

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