# FDA Inspection 1264951 - Defibtech, LLC - March 25, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/defibtech-llc/cb815974-b46a-4063-bd97-48d55f1a3753
Source feed: FDA_Inspections

> FDA Inspection 1264951 for Defibtech, LLC on March 25, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1264951
- Company Name: Defibtech, LLC
- Inspection Date: 2025-03-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1264951 - 2025-03-25](https://www.globalkeysolutions.net/records/fda_inspections/defibtech-llc/da0066b4-472d-4ebb-bf2a-bb4123114712)
- [FDA Inspection 1264951 - 2025-03-25](https://www.globalkeysolutions.net/records/fda_inspections/defibtech-llc/cf8f2eb1-4a8f-4ce6-91b6-32dce285e76c)
- [FDA Inspection 1264951 - 2025-03-25](https://www.globalkeysolutions.net/records/fda_inspections/defibtech-llc/c4f42356-f408-4872-af46-56faceac34c9)
- [FDA Inspection 1024231 - 2017-08-16](https://www.globalkeysolutions.net/records/fda_inspections/defibtech-llc/56a79898-db85-41bd-a509-14bf67ac81b9)

Company: https://www.globalkeysolutions.net/companies/defibtech-llc/4ebf10b2-dd7d-449a-979b-c65820d96663

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