# Bioptron AG – FDA Inspection, Nov 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/bioptron-ag/80a182b3-4902-475d-89ab-9f6e19186d53
Source feed: FDA_Inspections

> FDA inspection 1031661 of Bioptron AG, November 02, 2017. Classification: Voluntary Action Indicated (VAI). 12 citations under 21 CFR parts 803, 820 and 1002. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031661
- Company Name: Bioptron AG
- Inspection Date: 2017-11-02
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 12

## Related Officers

- [Investigator](https://www.keypedia.com/people/catherine-j-laufmann/920b7656-2847-408d-ba15-3989283d8c94)

Company: https://www.keypedia.com/companies/bioptron-ag/35b8f67d-a420-4f38-bbe4-32c75b23fc97

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