# Biomat USA Inc - Inspection Records

Source: https://www.keypedia.com/companies/biomat-usa-inc/bb09c108-6ef2-4a53-9a44-09d9196bc91c

> Inspection records and compliance data for Biomat USA Inc in Des Moines, Iowa. Access full analysis and detailed observations.

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## Details

- Name: Biomat USA Inc
- FEI Number: 3005601885
- City: Des Moines
- State: Iowa
- Country Name: United States
- Address Line 1: 1223 6th Ave
- Zip Code: 50314

## Related Documents

- [FDA Inspection 1196124 - Biomat USA Inc - 2023-01-13](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/1165d759-62df-4643-9551-0a0e56800e86) — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2023
- [FDA Inspection 1196124 - Biomat USA Inc - 2023-01-13](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/e06b21e9-562b-4ddc-970b-03802c8960c8) — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2023
- [FDA Inspection 1057142 - Biomat USA Inc - 2018-05-29](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/fb89d3cc-a810-42ef-a84c-71dfe08eb2ac) — classification: No Action Indicated (NAI), source: FDA, date: May 29, 2018
- [FDA Inspection 969080 - Biomat USA Inc - 2016-04-27](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/5eb5f302-444d-4243-9b98-45bc7b2f621a) — classification: No Action Indicated (NAI), source: FDA, date: April 27, 2016
- [FDA Inspection 867478 - Biomat USA Inc - 2014-02-24](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/a8e292f7-9831-4848-826a-bcfb3ee8f656) — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2014
- [FDA Inspection 753878 - Biomat USA Inc - 2011-11-18](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/9690f077-e246-4b2e-871f-ebb4268c05f4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 18, 2011
- [FDA Inspection 586398 - Biomat USA Inc - 2009-06-05](https://www.keypedia.com/records/fda_inspections/biomat-usa-inc/ecc33f92-1f64-41cd-8ec7-e5a39ac2a37b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 5, 2009

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