# FDA Inspection 1255908 - Immunexpress, Inc - December 06, 2024

Source: https://www.keypedia.com/records/fda_inspections/immunexpress-inc/6cab555a-e255-49b2-9283-ee8055b5ef99
Source feed: FDA_Inspections

> FDA Inspection 1255908 for Immunexpress, Inc on December 06, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1255908
- Company Name: Immunexpress, Inc
- Inspection Date: 2024-12-06
- 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 1255908 - 2024-12-06](https://www.keypedia.com/records/fda_inspections/immunexpress-inc/0ab15425-e3a6-4813-8c68-3003e448a437)
- [FDA Inspection 1255908 - 2024-12-06](https://www.keypedia.com/records/fda_inspections/immunexpress-inc/ed18edfd-83c6-4850-9ef2-8e0ce63a7693)
- [FDA Inspection 1255908 - 2024-12-06](https://www.keypedia.com/records/fda_inspections/immunexpress-inc/86eb3d39-09d8-4f36-90b1-1658ceb8c3e8)

Company: https://www.keypedia.com/companies/immunexpress-inc/95223a71-0912-48c3-b802-7f08b08af50b

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