# Biomat USA, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/biomat-usa-inc/edbd4f55-9776-4416-82ee-1a5c4aa49b2a

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

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## Details

- Name: Biomat USA, Inc.
- FEI Number: 3002793370
- City: Wichita Falls
- State: Texas
- Country Name: United States
- Address Line 1: 1908 9th St Ste D
- Zip Code: 76301

## Related Documents

- [483 - Biomat USA, Inc. - 2021-07-07](https://www.keypedia.com/records/483/biomat-usa-inc/a49556f4-9a54-4572-9e28-b4b70cab7e17) — source: FDA, date: July 7, 2021
- [FDA Inspection 1145751 - Biomat USA, Inc. - 2021-07-07](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/8b7c4910-7d5c-438c-86b3-da195e8f5cae) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 7, 2021
- [FDA Inspection 1145751 - Biomat USA, Inc. - 2021-07-07](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/e1d468b1-1767-46d0-9df7-f873d68a45fa) — classification: No Action Indicated (NAI), source: FDA, date: July 7, 2021
- [FDA Inspection 1028343 - Biomat USA, Inc. - 2017-09-20](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/790ee3db-9d74-40b3-9c18-498f31b344a1) — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2017
- [FDA Inspection 859643 - Biomat USA, Inc. - 2013-12-19](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/e216318f-8a58-45fd-9ef7-4cc1620ffc38) — classification: No Action Indicated (NAI), source: FDA, date: December 19, 2013
- [FDA Inspection 701934 - Biomat USA, Inc. - 2010-11-19](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/c6dced23-b5e0-4030-bd7b-859f0b1633ee) — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2010
- [FDA Inspection 557909 - Biomat USA, Inc. - 2009-01-15](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/24a2ce4d-a1bb-43eb-917d-06509b8ffc70) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 15, 2009

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