# PFM Medical Mepro GMBH – FDA Inspection, Jan 26, 2023

Source: https://www.keypedia.com/records/fda_inspections/pfm-medical-mepro-gmbh/3e620180-83ca-42c5-85bc-6b6594bae82b
Source feed: FDA_Inspections

> FDA inspection 1198107 of PFM Medical Mepro GMBH, January 26, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1067796 - 2018-08-30

## Related Officers

- [Joshua J. Silvestri](https://www.keypedia.com/people/joshua-j-silvestri/433e29b3-ce5f-44d2-9984-7a6cb61e1824)

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