# Koeze Company - Inspection Records

Source: https://www.globalkeysolutions.net/companies/koeze-company/f7e0c2d2-e347-4732-b6fc-4571725b842d

> Inspection records and compliance data for Koeze Company in Wyoming, Michigan. Access full analysis and detailed observations.

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## Details

- Name: Koeze Company
- FEI Number: 1810942
- City: Wyoming
- State: Michigan
- Country Name: United States
- Address Line 1: 2555 Burlingame Ave SW
- Zip Code: 49509

## Related Documents

- [FDA Inspection 992905 - Koeze Company - 2016-11-28](https://www.globalkeysolutions.net/records/fda_inspections/koeze-company/ea0e324e-03a0-4167-af9a-3fc5e1ecf27b) — classification: No Action Indicated (NAI), source: FDA, date: November 28, 2016
- [FDA Inspection 882927 - Koeze Company - 2014-06-13](https://www.globalkeysolutions.net/records/fda_inspections/koeze-company/3eec7b5c-a6b4-4aa2-afa3-224ea089b62d) — classification: No Action Indicated (NAI), source: FDA, date: June 13, 2014
- [FDA Inspection 882927 - Koeze Company - 2014-06-13](https://www.globalkeysolutions.net/records/fda_inspections/koeze-company/fd1494a6-7697-4218-a511-d433bdcfec59) — classification: No Action Indicated (NAI), source: FDA, date: June 13, 2014
- [FDA Inspection 882927 - Koeze Company - 2014-06-13](https://www.globalkeysolutions.net/records/fda_inspections/koeze-company/982e4065-7c50-48f0-a808-b8aca7fd934d) — classification: No Action Indicated (NAI), source: FDA, date: June 13, 2014
- [FDA Inspection 754283 - Koeze Company - 2011-11-21](https://www.globalkeysolutions.net/records/fda_inspections/koeze-company/9f5e061b-8698-46c8-9d67-9084a02aa936) — classification: No Action Indicated (NAI), source: FDA, date: November 21, 2011
- [FDA Inspection 674795 - Koeze Company - 2010-08-04](https://www.globalkeysolutions.net/records/fda_inspections/koeze-company/cfb0bfb6-3381-4ccd-a20d-125d47caa84b) — classification: No Action Indicated (NAI), source: FDA, date: August 4, 2010
- [FDA Inspection 611167 - Koeze Company - 2009-09-09](https://www.globalkeysolutions.net/records/fda_inspections/koeze-company/6f71565b-7625-46f0-998e-a1531d3a1d5e) — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2009

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