# Hemagen Diagnostics Inc – FDA Inspection, Jan 10, 2018

Source: https://www.keypedia.com/records/fda_inspections/hemagen-diagnostics-inc/9a37d426-9ef2-4c1c-b2bf-43581dce2e7f
Source feed: FDA_Inspections

> FDA inspection 1037233 of Hemagen Diagnostics Inc, January 10, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037233
- Company Name: Hemagen Diagnostics Inc
- Inspection Date: 2018-01-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

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## Related Officers

- [Company Rep](https://www.keypedia.com/people/james-m-simpson/3c0113ae-d846-4e37-aafa-13d58c465fa3)

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