# FDA Inspection 1288958 - JenaValve Technology, Inc. - October 10, 2025

Source: https://www.keypedia.com/records/fda_inspections/jenavalve-technology-inc/f03c8bb4-15af-48a6-b1de-ef7cfdf97b6c
Source feed: FDA_Inspections

> FDA Inspection 1288958 for JenaValve Technology, Inc. on October 10, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1288958
- Company Name: JenaValve Technology, Inc.
- Inspection Date: 2025-10-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1302684 - 2026-01-15](https://www.keypedia.com/records/fda_inspections/jenavalve-technology-inc/4e5e33ca-aaed-485c-b0df-44c2efa5320a)
- [FDA Inspection 1288958 - 2025-10-10](https://www.keypedia.com/records/fda_inspections/jenavalve-technology-inc/a05011d3-da9b-41d3-a7a9-cf41241b3b9e)

Company: https://www.keypedia.com/companies/jenavalve-technology-inc/ce94d14f-14b8-443e-823f-f5558609dbec

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