# FDA Inspection 1198107 - PFM Medical Mepro GMBH - January 26, 2023

Source: https://www.keypedia.com/records/fda_inspections/pfm-medical-mepro-gmbh/2ac7f91f-fd3a-4197-8905-e094207fb541
Source feed: FDA_Inspections

> FDA Inspection 1198107 for PFM Medical Mepro GMBH on January 26, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1198107
- Company Name: PFM Medical Mepro GMBH
- Inspection Date: 2023-01-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1198107 - 2023-01-26](https://www.keypedia.com/records/fda_inspections/pfm-medical-mepro-gmbh/3e620180-83ca-42c5-85bc-6b6594bae82b)

Company: https://www.keypedia.com/companies/pfm-medical-mepro-gmbh/8f86301c-eaec-49c7-a943-08e8c5965211

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