# Simex Medizintechnik Gmbh – FDA Inspection, Nov 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/simex-medizintechnik-gmbh/b4477be9-9d78-40c9-89d2-8725d79ef6d3
Source feed: FDA_Inspections

> FDA inspection 1031382 of Simex Medizintechnik Gmbh, November 15, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031382
- Company Name: Simex Medizintechnik Gmbh
- Inspection Date: 2017-11-15
- 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: 1

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## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

Company: https://www.keypedia.com/companies/simex-medizintechnik-gmbh/e6a56605-72a2-44cd-91ea-2d65fa683e05

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