# Medi-Globe GmbH – FDA Inspection, Oct 20, 2010

Source: https://www.keypedia.com/records/fda_inspections/medi-globe-gmbh/a174cab2-6071-4664-aed6-a89916860e0a
Source feed: FDA_Inspections

> FDA inspection 698625 of Medi-Globe GmbH, October 20, 2010. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 698625
- Company Name: Medi-Globe GmbH
- Inspection Date: 2010-10-20
- 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: 3

## Related Documents

- FDA Inspection 917419 - 2015-02-18

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
