# FDA Inspection 1110573 - Drucker Diagnostics - November 21, 2019

Source: https://www.keypedia.com/records/fda_inspections/drucker-diagnostics/8ebe924c-06f2-4b07-b01e-16d934a60f56
Source feed: FDA_Inspections

> FDA Inspection 1110573 for Drucker Diagnostics on November 21, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1110573
- Company Name: Drucker Diagnostics
- Inspection Date: 2019-11-21
- 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/drucker-diagnostics/408b6c9a-dd6f-4680-abb7-0933a6163552

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