# FDA Inspection 934613 - Mevis Medical Solutions AG - June 24, 2015

Source: https://www.keypedia.com/records/fda_inspections/mevis-medical-solutions-ag/5c1bfdd6-217d-4dbd-a37e-8f1212b02e08
Source feed: FDA_Inspections

> FDA Inspection 934613 for Mevis Medical Solutions AG on June 24, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 934613
- Company Name: Mevis Medical Solutions AG
- Inspection Date: 2015-06-24
- 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 934613 - 2015-06-24](https://www.keypedia.com/records/fda_inspections/mevis-medical-solutions-ag/0588ebc0-a217-461a-917f-2192a54c9591)

Company: https://www.keypedia.com/companies/mevis-medical-solutions-ag/a2858b95-9a1a-496c-9b0c-cbc92bfb6c02

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