# FDA Inspection 1097388 - Leonhard Lang Medizintechnik GmbH - July 24, 2019

Source: https://www.keypedia.com/records/fda_inspections/leonhard-lang-medizintechnik-gmbh/1f965b2d-c37d-4176-9239-2e06a7816250
Source feed: FDA_Inspections

> FDA Inspection 1097388 for Leonhard Lang Medizintechnik GmbH on July 24, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1097388
- Company Name: Leonhard Lang Medizintechnik GmbH
- Inspection Date: 2019-07-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 906898 - 2014-11-20](https://www.keypedia.com/records/fda_inspections/leonhard-lang-medizintechnik-gmbh/5f769eee-8ea1-422c-9e6b-042230716969)
- [FDA Inspection 906898 - 2014-11-20](https://www.keypedia.com/records/fda_inspections/leonhard-lang-medizintechnik-gmbh/9ec09e64-52fe-4442-a0d0-53e507643847)

Company: https://www.keypedia.com/companies/leonhard-lang-medizintechnik-gmbh/91a743fa-0ce3-4b8d-baa3-005c593e9a5c

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