# BioZyme, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/biozyme-inc/0c2ed2af-88f5-460c-8341-7e421517b237

> Inspection records and compliance data for BioZyme, Inc. in Saint Joseph, Missouri. Access full analysis and detailed observations.

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## Details

- Name: BioZyme, Inc.
- FEI Number: 1931140
- City: Saint Joseph
- State: Missouri
- Country Name: United States
- Address Line 1: 4621 Easton Rd
- Zip Code: 64503

## Related Documents

- [FDA Inspection 1279788 - BioZyme, Inc. - 2025-08-18](https://www.globalkeysolutions.net/records/fda_inspections/biozyme-inc/0c64cf8f-1b55-4325-8df7-f34d18a476e1) — source: FDA, date: August 18, 2025
- [FDA Inspection 1279788 - BioZyme, Inc. - 2025-08-18](https://www.globalkeysolutions.net/records/fda_inspections/biozyme-inc/7156b5b2-d649-4445-84bf-5edaef928e3d) — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2025
- [FDA Inspection 980111 - BioZyme, Inc. - 2016-07-14](https://www.globalkeysolutions.net/records/fda_inspections/biozyme-inc/4cf0000e-a753-4acb-b554-eb6850de01fe) — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2016
- [FDA Inspection 870017 - BioZyme, Inc. - 2013-08-23](https://www.globalkeysolutions.net/records/fda_inspections/biozyme-inc/de8b1ef2-b945-4ea0-b94b-05d5f70f1a12) — classification: No Action Indicated (NAI), source: FDA, date: August 23, 2013
- [FDA Inspection 809383 - BioZyme, Inc. - 2012-11-19](https://www.globalkeysolutions.net/records/fda_inspections/biozyme-inc/10d934a5-764b-48e0-89f0-5fe4e0cd64d2) — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2012
- [FDA Inspection 762553 - BioZyme, Inc. - 2012-01-09](https://www.globalkeysolutions.net/records/fda_inspections/biozyme-inc/9a287314-8b8f-49e3-9394-2293bb8b0ef6) — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2012
- [FDA Inspection 578771 - BioZyme, Inc. - 2009-04-21](https://www.globalkeysolutions.net/records/fda_inspections/biozyme-inc/ef7912eb-3768-45bb-9513-cdb7b5381d19) — classification: Official Action Indicated (OAI), source: FDA, date: April 21, 2009

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