# Biomat USA Inc - Inspection Records

Source: https://www.keypedia.com/companies/biomat-usa-inc/5fbf4b45-3297-4af5-965b-4af7849ed313

> Inspection records and compliance data for Biomat USA Inc in Lafayette, Louisiana. Access full analysis and detailed observations.

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## Details

- Name: Biomat USA Inc
- FEI Number: 2376147
- City: Lafayette
- State: Louisiana
- Country Name: United States
- Address Line 1: 325 E Main St
- Zip Code: 70501

## Related Documents

- [483 - Biomat USA Inc - 2023-04-04](https://www.keypedia.com/records/483/biomat-usa-inc/920d3db4-fd77-48f1-8b53-84c2a9cae56d) — source: FDA, date: April 4, 2023
- [FDA Inspection 1201897 - Biomat USA Inc - 2023-04-04](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/ef25939f-3997-49f7-84bc-013f0d54a86d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 4, 2023
- [FDA Inspection 1201897 - Biomat USA Inc - 2023-04-04](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/b800975c-70f8-4652-a042-511ed2ca3630) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 4, 2023
- [FDA Inspection 1009373 - Biomat USA Inc - 2017-04-28](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/1ac2eed8-15ac-4607-aea8-7a50b23c0fc4) — classification: No Action Indicated (NAI), source: FDA, date: April 28, 2017
- [FDA Inspection 885925 - Biomat USA Inc - 2014-07-01](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/de6b23f3-2099-4b55-9919-5f923d43ab9d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 1, 2014
- [FDA Inspection 760159 - Biomat USA Inc - 2011-12-21](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/e23c9047-5a68-4f54-be7c-ad7d70ff3f9d) — classification: No Action Indicated (NAI), source: FDA, date: December 21, 2011
- [FDA Inspection 578325 - Biomat USA Inc - 2009-04-24](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/5ba650f2-8461-4566-914b-fba86afd36e8) — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2009

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