# FDA Inspection 1194137 - Dornier Medtech Systems GmbH - December 14, 2022

Source: https://www.keypedia.com/records/fda_inspections/dornier-medtech-systems-gmbh/046672bb-850c-4fb7-983c-934e2e169dbe
Source feed: FDA_Inspections

> FDA Inspection 1194137 for Dornier Medtech Systems GmbH on December 14, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1194137
- Company Name: Dornier Medtech Systems GmbH
- Inspection Date: 2022-12-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1194137 - 2022-12-14](https://www.keypedia.com/records/fda_inspections/dornier-medtech-systems-gmbh/52647d3a-70ef-4a59-94e0-064a96980bbc)
- [FDA Inspection 726892 - 2011-04-29](https://www.keypedia.com/records/fda_inspections/dornier-medtech-systems-gmbh/e2206f27-14ff-449b-82c4-402633933d42)
- [FDA Inspection 726892 - 2011-04-29](https://www.keypedia.com/records/fda_inspections/dornier-medtech-systems-gmbh/fa64b0d1-39ab-4165-b4c1-678ece67fdb3)

Company: https://www.keypedia.com/companies/dornier-medtech-systems-gmbh/c0c5cabc-b89f-4ca5-9146-659dbfd4f750

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