# Somatex Medical Technologies GMBH – FDA Inspection, Nov 6, 2019

Source: https://www.keypedia.com/records/fda_inspections/somatex-medical-technologies-gmbh/9e0b8e6c-de90-47a8-8237-7b7f062ee71a
Source feed: FDA_Inspections

> FDA inspection 1108917 of Somatex Medical Technologies GMBH, November 06, 2019. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1108917
- Company Name: Somatex Medical Technologies GMBH
- Inspection Date: 2019-11-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 941408 - 2015-09-10
- [FDA Inspection 899832 - 2014-10-16](https://www.keypedia.com/records/fda_inspections/somatex-medical-technologies-gmbh/29cf824c-d019-4fb0-95ab-ce38f941e1c2)

Company: https://www.keypedia.com/companies/somatex-medical-technologies-gmbh/5225948d-3741-46de-9643-9571e652d5ed

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