# FDA Inspection 1266030 - Cognivue Inc. - June 13, 2025

Source: https://www.keypedia.com/records/fda_inspections/cognivue-inc/770b2e5e-574d-4436-b08d-76126b18234e
Source feed: FDA_Inspections

> FDA Inspection 1266030 for Cognivue Inc. on June 13, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1266030
- Company Name: Cognivue Inc.
- Inspection Date: 2025-06-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New York District Office

## Related Documents

- [FDA Inspection 1266030 - 2025-06-13](https://www.keypedia.com/records/fda_inspections/cognivue-inc/287c9a8f-e28f-4e7d-a7e4-103d8a2f9d0d)
- [FDA Inspection 1266030 - 2025-06-13](https://www.keypedia.com/records/fda_inspections/cognivue-inc/90fbc487-6785-4655-8983-e30d9b04a4ce)
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- [FDA Inspection 1177892 - 2022-08-15](https://www.keypedia.com/records/fda_inspections/cognivue-inc/ce6cc066-29c7-48d5-b962-92f9ceeebbd3)
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Company: https://www.keypedia.com/companies/cognivue-inc/12d584b2-cd96-4b0f-9d92-6efb90102a80

Office: https://www.keypedia.com/offices/new-york-district-office/9fa3d265-16ca-438d-8a6e-b47f60dc260d
