# Biomat USA, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/biomat-usa-inc/21a3c056-72f5-4064-ba8d-41c59b7fef6a

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

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## Details

- Name: Biomat USA, Inc.
- FEI Number: 1044773
- City: Clarksville
- State: Tennessee
- Country Name: United States
- Address Line 1: 1596 Fort Campbell Blvd Ste C
- Zip Code: 37042

## Related Documents

- [FDA Inspection 1254129 - Biomat USA, Inc. - 2024-11-08](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/60317ec8-26dc-4a7e-b911-e3a0d9941898) — source: FDA, date: November 8, 2024
- [FDA Inspection 1254129 - Biomat USA, Inc. - 2024-11-08](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/cffa8c98-6cb9-40d1-a99f-68457245a199) — classification: No Action Indicated (NAI), source: FDA, date: November 8, 2024
- [FDA Inspection 1099928 - Biomat USA, Inc. - 2019-08-07](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/2112f251-c2f4-4a51-9de6-e0668a44130f) — classification: No Action Indicated (NAI), source: FDA, date: August 7, 2019
- [FDA Inspection 1034540 - Biomat USA, Inc. - 2017-10-25](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/91c40358-0f8f-4168-950b-1e122fa0db17) — classification: No Action Indicated (NAI), source: FDA, date: October 25, 2017
- [FDA Inspection 980726 - Biomat USA, Inc. - 2016-06-21](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/3375abfd-cbab-48ee-a027-48ecb97b833e) — classification: No Action Indicated (NAI), source: FDA, date: June 21, 2016
- [FDA Inspection 857568 - Biomat USA, Inc. - 2013-11-20](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/069b20a2-570a-4dca-88c6-a74193d7512e) — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2013
- [FDA Inspection 646575 - Biomat USA, Inc. - 2010-02-08](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/b88fa37e-72be-461f-8e91-e01cfbadf006) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 8, 2010

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