# FDA Inspection 864721 - Moeller Medical GmbH - January 30, 2014

Source: https://www.keypedia.com/records/fda_inspections/moeller-medical-gmbh/1f47d58e-26c5-4fa2-a7bd-35283cefb13a
Source feed: FDA_Inspections

> FDA Inspection 864721 for Moeller Medical GmbH on January 30, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 864721
- Company Name: Moeller Medical GmbH
- Inspection Date: 2014-01-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1203595 - 2023-03-30](https://www.keypedia.com/records/fda_inspections/moeller-medical-gmbh/29db04b8-fffe-4517-a5ba-812cdd8f5e4f)
- [FDA Inspection 864721 - 2014-01-30](https://www.keypedia.com/records/fda_inspections/moeller-medical-gmbh/e11a58d6-aefc-4c55-8d24-3a09fecabe81)

Company: https://www.keypedia.com/companies/moeller-medical-gmbh/416c5a80-cba8-450f-8334-42a9e223c093

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