# FDA Inspection 914852 - MedFact Engineering GmbH - February 12, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/medfact-engineering-gmbh/14e38495-dce6-4a23-a88d-790ed7aa9703
Source feed: FDA_Inspections

> FDA Inspection 914852 for MedFact Engineering GmbH on February 12, 2015. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 914852
- Company Name: MedFact Engineering GmbH
- Inspection Date: 2015-02-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1199206 - 2023-02-16](https://www.globalkeysolutions.net/records/fda_inspections/medfact-engineering-gmbh/c74db8aa-dd36-4c02-8f4c-271ef6931dab)
- [FDA Inspection 1063787 - 2018-07-25](https://www.globalkeysolutions.net/records/fda_inspections/medfact-engineering-gmbh/fce69e94-e30e-462b-9918-12cb16a3d88f)
- [FDA Inspection 914852 - 2015-02-12](https://www.globalkeysolutions.net/records/fda_inspections/medfact-engineering-gmbh/ba6db906-d0af-4698-ad26-92a5c12071ad)

Company: https://www.globalkeysolutions.net/companies/medfact-engineering-gmbh/753076b5-c98d-4257-9f98-d4cb6df7ae51

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