# IRT Systems GmbH – FDA Inspection, Jun 16, 2017

Source: https://www.keypedia.com/records/fda_inspections/irt-systems-gmbh/7e726fef-bca3-40ee-9539-bb9f263c155e
Source feed: FDA_Inspections

> FDA inspection 1020729 of IRT Systems GmbH, June 16, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020729
- Company Name: IRT Systems GmbH
- Inspection Date: 2017-06-16
- 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 Officers

- [Issuing Officer](https://www.keypedia.com/people/jacqueline-s-warner/d001f4ec-db46-4d78-a5dd-efea7ddfb893)

Company: https://www.keypedia.com/companies/irt-systems-gmbh/581bce35-1647-43fa-9040-8bb95ef137e3

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