# Somatex Medical Technologies GMBH - Inspection Records

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

> Inspection records and compliance data for Somatex Medical Technologies GMBH in Berlin, None. Access full analysis and detailed observations.

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## Details

- Name: Somatex Medical Technologies GMBH
- FEI Number: 1000408433
- City: Berlin
- State: None
- Country Name: Germany
- Address Line 1: Hohenzollerndamm 150-151
- Zip Code: None

## Related Documents

- [FDA Inspection 1108917 - Somatex Medical Technologies GMBH - 2019-11-06](https://www.keypedia.com/records/fda_inspections/somatex-medical-technologies-gmbh/9e0b8e6c-de90-47a8-8237-7b7f062ee71a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 6, 2019
- [FDA Inspection 1108917 - Somatex Medical Technologies GMBH - 2019-11-06](https://www.keypedia.com/records/fda_inspections/somatex-medical-technologies-gmbh/230b4da3-14fe-42e5-ad3e-a73e65dd59f5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 6, 2019
- [FDA Inspection 941408 - Somatex Medical Technologies GMBH - 2015-09-10](https://www.keypedia.com/records/fda_inspections/somatex-medical-technologies-gmbh/4ad5d322-37fe-46d3-a0c6-140fd9736335) — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2015
- [FDA Inspection 941408 - Somatex Medical Technologies GMBH - 2015-09-10](https://www.keypedia.com/records/fda_inspections/somatex-medical-technologies-gmbh/f9dafe31-abd8-4216-82df-392a50e56496) — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2015
- [WARNING_LETTER - Somatex Medical Technologies GMBH - 2014-10-16](https://www.keypedia.com/records/warning_letter/somatex-medical-technologies-gmbh/f8fbbe69-3690-4981-9aa3-e3251bdb80e7) — source: FDA, date: October 16, 2014
- [FDA Inspection 899832 - Somatex Medical Technologies GMBH - 2014-10-16](https://www.keypedia.com/records/fda_inspections/somatex-medical-technologies-gmbh/29cf824c-d019-4fb0-95ab-ce38f941e1c2) — classification: Official Action Indicated (OAI), source: FDA, date: October 16, 2014

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