# FDA Inspection 1031660 - Bioptron AG - November 01, 2017

Source: https://www.keypedia.com/records/fda_inspections/bioptron-ag/07f1c13f-6f11-4006-a120-2fe91af93781
Source feed: FDA_Inspections

> FDA Inspection 1031660 for Bioptron AG on November 01, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031660
- Company Name: Bioptron AG
- Inspection Date: 2017-11-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/bioptron-ag/0725d454-f364-4da2-ba85-600b6e7cddde

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