# FDA Inspection 1279102 - Kaohinani Longwolf, MD - August 13, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/kaohinani-longwolf-md/d9647801-f091-4c9c-8d67-ccad609147db
Source feed: FDA_Inspections

> FDA Inspection 1279102 for Kaohinani Longwolf, MD on August 13, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1279102
- Company Name: Kaohinani Longwolf, MD
- Inspection Date: 2025-08-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1279102 - 2025-08-13](https://www.globalkeysolutions.net/records/fda_inspections/kaohinani-longwolf-md/77d73798-721f-4c53-8b5d-252cff44adce)

Company: https://www.globalkeysolutions.net/companies/kaohinani-longwolf-md/edf5ce61-6038-4ec8-ba7d-0f70a84fbcb1

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