# FDA Inspection 1256493 - Medshift - December 13, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/medshift/8a191fb5-2832-47af-8375-cdd5d2f6791b
Source feed: FDA_Inspections

> FDA Inspection 1256493 for Medshift on December 13, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1256493
- Company Name: Medshift
- Inspection Date: 2024-12-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1256493 - 2024-12-13](https://www.globalkeysolutions.net/records/fda_inspections/medshift/4b244b39-53e1-4c8d-8510-a2a1ca3f211a)
- [FDA Inspection 1256493 - 2024-12-13](https://www.globalkeysolutions.net/records/fda_inspections/medshift/14c0190d-6965-443d-b451-2ef5e1f89bb5)
- [FDA Inspection 1256493 - 2024-12-13](https://www.globalkeysolutions.net/records/fda_inspections/medshift/cb6ff8a0-4db5-4bc9-b8e7-18608e748b2b)

Company: https://www.globalkeysolutions.net/companies/medshift/179abcc0-cbc6-466e-ae15-bf33fa8e14df

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