# LRE Medical GmbH – FDA Inspection, Jul 26, 2018

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

> FDA inspection 1061475 of LRE Medical GmbH, July 26, 2018. Classification: Voluntary Action Indicated (VAI). 3 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: 1061475
- Company Name: LRE Medical GmbH
- Inspection Date: 2018-07-26
- 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: 3

## Related Documents

- FDA Inspection 1012391 - 2017-02-03

## Related Officers

- [Investigator](https://www.keypedia.com/people/nydia-e-colon/c5137ded-6ae7-4855-b5b3-113bd851e1c3)

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

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