# Hemagen Diagnostics Inc – FDA Inspection, May 14, 2026

Source: https://www.keypedia.com/records/fda_inspections/hemagen-diagnostics-inc/93b62636-b780-4484-82a8-1062f5f511f3
Source feed: FDA_Inspections

> FDA inspection 1317040 of Hemagen Diagnostics Inc, May 14, 2026. Classification: Voluntary Action Indicated (VAI). 5 citations. Form 483 issued. 5 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- FDA Inspection 1208393 - 2023-06-14
- [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
- [FDA Inspection 812190 - 2012-12-20](https://www.keypedia.com/records/fda_inspections/hemagen-diagnostics-inc/7e05ce43-8147-4113-97e7-05b629a63144)
- FDA Inspection 677299 - 2010-08-25

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/christina-d-mello/b523622e-d2dd-4ff6-9b2b-74b3134841de)

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