# FDA Inspection 1000150 - LMT MEDICAL SYSTEMS GMBH - January 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/lmt-medical-systems-gmbh/a02bef28-fbec-4504-99f1-a880d453eb91
Source feed: FDA_Inspections

> FDA Inspection 1000150 for LMT MEDICAL SYSTEMS GMBH on January 19, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000150
- Company Name: LMT MEDICAL SYSTEMS GMBH
- Inspection Date: 2017-01-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1234658 - 2024-02-15](https://www.keypedia.com/records/fda_inspections/lmt-medical-systems-gmbh/91019390-5677-4874-811b-e28b89c1152f)

Company: https://www.keypedia.com/companies/lmt-medical-systems-gmbh/945d9461-e10b-4449-9437-445b0776507b

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