# Hemedex, Inc. – FDA Inspection, Oct 5, 2017

Source: https://www.keypedia.com/records/fda_inspections/hemedex-inc/e42fbca6-8e08-49c5-b65a-0e034fefbc47
Source feed: FDA_Inspections

> FDA inspection 1028218 of Hemedex, Inc., October 05, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028218
- Company Name: Hemedex, Inc.
- Inspection Date: 2017-10-05
- 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: 1

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## Related Officers

- [Company Rep](https://www.keypedia.com/people/james-p-finn/70e5c36c-2711-449b-bf73-e08b4dd58449)

Company: https://www.keypedia.com/companies/hemedex-inc/be6a1de7-58a9-4676-9f24-3aa38a88a7f4

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