# Moeller Medical GmbH – FDA Inspection, Mar 30, 2023

Source: https://www.keypedia.com/records/fda_inspections/moeller-medical-gmbh/29db04b8-fffe-4517-a5ba-812cdd8f5e4f
Source feed: FDA_Inspections

> FDA inspection 1203595 of Moeller Medical GmbH, March 30, 2023. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1203595
- Company Name: Moeller Medical GmbH
- Inspection Date: 2023-03-30
- 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: 0

## Related Documents

- [FDA Inspection 1087392 - 2018-03-22](https://www.keypedia.com/records/fda_inspections/moeller-medical-gmbh/c5185da0-50b6-43e7-b2b7-522c5a17390a)
- [FDA Inspection 864721 - 2014-01-30](https://www.keypedia.com/records/fda_inspections/moeller-medical-gmbh/e11a58d6-aefc-4c55-8d24-3a09fecabe81)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

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