# FDA Inspection 1292692 - PRENOSIS INC - November 19, 2025

Source: https://www.keypedia.com/records/fda_inspections/prenosis-inc/dab8ff38-08eb-4b28-a827-2eae2e4451d2
Source feed: FDA_Inspections

> FDA Inspection 1292692 for PRENOSIS INC on November 19, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1292692
- Company Name: PRENOSIS INC
- Inspection Date: 2025-11-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Chicago District Office

## Related Documents

- [FDA Inspection 1292692 - 2025-11-19](https://www.keypedia.com/records/fda_inspections/prenosis-inc/2ede7d7e-3d21-40bf-86ca-7296bc36cfcb)
- [FDA Inspection 1292692 - 2025-11-19](https://www.keypedia.com/records/fda_inspections/prenosis-inc/3b4ef91a-afa9-4b8b-a551-ea025d7a2675)
- [FDA Inspection 1292692 - 2025-11-19](https://www.keypedia.com/records/fda_inspections/prenosis-inc/73326473-da8c-4f7d-8fb3-1c5f53a50779)

Company: https://www.keypedia.com/companies/prenosis-inc/9225f87c-16ce-4c76-8e29-d1f4c52b8fbb

Office: https://www.keypedia.com/offices/chicago-district-office/a510300b-0eaf-4a33-90b5-231d95977669