# FDA Inspection 1317040 - Hemagen Diagnostics Inc - May 14, 2026

Source: https://www.keypedia.com/records/fda_inspections/hemagen-diagnostics-inc/20bb5642-0ae1-46d9-9cde-e8506784a2a8
Source feed: FDA_Inspections

> FDA Inspection 1317040 for Hemagen Diagnostics Inc on May 14, 2026. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1317040
- Company Name: Hemagen Diagnostics Inc
- Inspection Date: 2026-05-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1317040 - 2026-05-14](https://www.keypedia.com/records/fda_inspections/hemagen-diagnostics-inc/93b62636-b780-4484-82a8-1062f5f511f3)
- [FDA Inspection 1208393 - 2023-06-14](https://www.keypedia.com/records/fda_inspections/hemagen-diagnostics-inc/6ca18e9c-d25f-4874-9a14-f052af448bd8)
- [FDA Inspection 1037233 - 2018-01-10](https://www.keypedia.com/records/fda_inspections/hemagen-diagnostics-inc/9a37d426-9ef2-4c1c-b2bf-43581dce2e7f)
- [FDA Inspection 918077 - 2015-03-10](https://www.keypedia.com/records/fda_inspections/hemagen-diagnostics-inc/4cf6218b-6691-4c3a-beda-c3a3f848f9e3)
- [FDA Inspection 918077 - 2015-03-10](https://www.keypedia.com/records/fda_inspections/hemagen-diagnostics-inc/bcce5480-65c7-464e-86d0-f6a3e550802c)

Company: https://www.keypedia.com/companies/hemagen-diagnostics-inc/ecf17e24-e402-4def-8b3a-6d7e68e19be2

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7