# Hemedex, Inc. – FDA Inspection, Aug 19, 2026

Source: https://www.keypedia.com/records/fda_inspections/hemedex-inc/49e044fe-98c4-4fa7-acd5-2700b654aea2
Source feed: FDA_Inspections

> FDA inspection 1333962 of Hemedex, Inc., August 19, 2026. Classification: No Action Indicated (NAI). 3 citations. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1333962
- Company Name: Hemedex, Inc.
- Inspection Date: 2026-08-19
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1207959 - 2023-02-17
- [FDA Inspection 1028218 - 2017-10-05](https://www.keypedia.com/records/fda_inspections/hemedex-inc/e42fbca6-8e08-49c5-b65a-0e034fefbc47)
- [FDA Inspection 822744 - 2013-03-14](https://www.keypedia.com/records/fda_inspections/hemedex-inc/921222cf-516b-41db-97f3-39d5a0508ffb)
- FDA Inspection 667620 - 2010-06-10

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