# FDA Inspection 1031661 - Bioptron AG - November 02, 2017

Source: https://www.keypedia.com/records/fda_inspections/bioptron-ag/64a6b3f7-060c-4ef5-8887-84acf699a633
Source feed: FDA_Inspections

> FDA Inspection 1031661 for Bioptron AG on November 02, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1031661 - 2017-11-02](https://www.keypedia.com/records/fda_inspections/bioptron-ag/80a182b3-4902-475d-89ab-9f6e19186d53)

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