# FDA Inspection 1115022 - Simple Diagnostics, Inc. - January 08, 2020

Source: https://www.keypedia.com/records/fda_inspections/simple-diagnostics-inc/16fc8be3-163f-490e-b18b-8fcc480cdf19
Source feed: FDA_Inspections

> FDA Inspection 1115022 for Simple Diagnostics, Inc. on January 08, 2020. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1115022
- Company Name: Simple Diagnostics, Inc.
- Inspection Date: 2020-01-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1128795 - 2020-08-25](https://www.keypedia.com/records/fda_inspections/simple-diagnostics-inc/9508f3e0-145f-4ad1-9acb-d240a9ada1ff)
- [FDA Inspection 1115022 - 2020-01-08](https://www.keypedia.com/records/fda_inspections/simple-diagnostics-inc/ce37fa7e-c0b1-42bf-b80f-47049c901fc0)

Company: https://www.keypedia.com/companies/simple-diagnostics-inc/a1507838-f54e-494c-bd14-1f503e3cad28

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