# FDA Inspection 1092548 - Cognivue Inc. - June 04, 2019

Source: https://www.keypedia.com/records/fda_inspections/cognivue-inc/f62b9129-e202-497e-9eba-5b785fab9b43
Source feed: FDA_Inspections

> FDA Inspection 1092548 for Cognivue Inc. on June 04, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1092548
- Company Name: Cognivue Inc.
- Inspection Date: 2019-06-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/cognivue-inc/12d584b2-cd96-4b0f-9d92-6efb90102a80

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