# FDA Inspection 917419 - Medi-Globe GmbH - February 18, 2015

Source: https://www.keypedia.com/records/fda_inspections/medi-globe-gmbh/7204a90c-3619-466c-95d8-a80ba9f244f3
Source feed: FDA_Inspections

> FDA Inspection 917419 for Medi-Globe GmbH on February 18, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 917419
- Company Name: Medi-Globe GmbH
- Inspection Date: 2015-02-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 917419 - 2015-02-18](https://www.keypedia.com/records/fda_inspections/medi-globe-gmbh/77920ebc-b282-4aa4-9752-d335adf230fe)
- [FDA Inspection 698625 - 2010-10-20](https://www.keypedia.com/records/fda_inspections/medi-globe-gmbh/32d39c4b-4b4b-40ad-b239-1c444b08ace0)
- [FDA Inspection 698625 - 2010-10-20](https://www.keypedia.com/records/fda_inspections/medi-globe-gmbh/a174cab2-6071-4664-aed6-a89916860e0a)

Company: https://www.keypedia.com/companies/medi-globe-gmbh/bfdf047e-8681-4a52-9c6d-ec5885674c07

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