# Aristotech Industries GmbH – FDA Inspection, Aug 30, 2018

Source: https://www.keypedia.com/records/fda_inspections/aristotech-industries-gmbh/7d65e121-77c4-4263-99e7-615f2347a83f
Source feed: FDA_Inspections

> FDA inspection 1064236 of Aristotech Industries GmbH, August 30, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1064236
- Company Name: Aristotech Industries GmbH
- Inspection Date: 2018-08-30
- 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: 4

## Related Officers

- [Investigator](https://www.keypedia.com/people/ashley-a-mutawakkil/512be391-fd96-451c-9569-98e43cfba9db)

Company: https://www.keypedia.com/companies/aristotech-industries-gmbh/7b0c7cf0-4e58-40ce-bafb-198a78769e61

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