# FDA Inspection 1061475 - LRE Medical GmbH - July 26, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/lre-medical-gmbh/45f4076b-6e63-479c-b67d-f2af26ff6db0
Source feed: FDA_Inspections

> FDA Inspection 1061475 for LRE Medical GmbH on July 26, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1061475
- Company Name: LRE Medical GmbH
- Inspection Date: 2018-07-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1012391 - 2017-02-03](https://www.globalkeysolutions.net/records/fda_inspections/lre-medical-gmbh/376b49f0-d54c-4732-95bb-8583a71d9851)

Company: https://www.globalkeysolutions.net/companies/lre-medical-gmbh/253e3a2e-bc30-4610-a9eb-faa9b19bd4b1

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