# LMT MEDICAL SYSTEMS GMBH – FDA Inspection, Jan 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 of LMT MEDICAL SYSTEMS GMBH, January 19, 2017. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- 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: 9

## Related Documents

- FDA Inspection 1234658 - 2024-02-15

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

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