# Leonhard Lang Medizintechnik GmbH – FDA Inspection, Jul 24, 2019

Source: https://www.keypedia.com/records/fda_inspections/leonhard-lang-medizintechnik-gmbh/a6905f45-2a8e-46b4-b063-b072f4a56841
Source feed: FDA_Inspections

> FDA inspection 1097388 of Leonhard Lang Medizintechnik GmbH, July 24, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1097388
- Company Name: Leonhard Lang Medizintechnik GmbH
- Inspection Date: 2019-07-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

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

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

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