# FDA Inspection 1097561 - DB Diagnostic Systems Inc. - July 16, 2019

Source: https://www.keypedia.com/records/fda_inspections/db-diagnostic-systems-inc/618e200e-e023-4824-9a2e-ccee4cfbfac4
Source feed: FDA_Inspections

> FDA Inspection 1097561 for DB Diagnostic Systems Inc. on July 16, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097561
- Company Name: DB Diagnostic Systems Inc.
- Inspection Date: 2019-07-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1192146 - 2022-12-05](https://www.keypedia.com/records/fda_inspections/db-diagnostic-systems-inc/970883fc-505e-4402-916c-4b4981eee847)
- [FDA Inspection 1192146 - 2022-12-05](https://www.keypedia.com/records/fda_inspections/db-diagnostic-systems-inc/43fefac2-7103-432f-8a4c-dd5ac7493ac9)
- [FDA Inspection 1097561 - 2019-07-16](https://www.keypedia.com/records/fda_inspections/db-diagnostic-systems-inc/3d453a93-59ee-4576-83e6-07cc11fa8296)

Company: https://www.keypedia.com/companies/db-diagnostic-systems-inc/6f86a3f8-b271-4caf-ba5c-ee52dee53045

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