# FDA Inspection 1176368 - 3DPX Medical - July 28, 2022

Source: https://www.keypedia.com/records/fda_inspections/3dpx-medical/8f6e2ed7-c06d-42be-a8d2-09b028782dda
Source feed: FDA_Inspections

> FDA Inspection 1176368 for 3DPX Medical on July 28, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1176368
- Company Name: 3DPX Medical
- Inspection Date: 2022-07-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1176368 - 2022-07-28](https://www.keypedia.com/records/fda_inspections/3dpx-medical/06d558cb-7dc3-49af-864e-02e9d7aba294)

Company: https://www.keypedia.com/companies/3dpx-medical/0cb0cecb-e3a4-4d00-a3a3-fab73a9eca85

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