# FDA Inspection 1267173 - Arboleaf Corporation - April 18, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/arboleaf-corporation/ade3682a-ddea-4882-9eeb-e9bbd2efebfb
Source feed: FDA_Inspections

> FDA Inspection 1267173 for Arboleaf Corporation on April 18, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1267173
- Company Name: Arboleaf Corporation
- Inspection Date: 2025-04-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1267173 - 2025-04-18](https://www.globalkeysolutions.net/records/fda_inspections/arboleaf-corporation/36edcb78-d827-45bb-9ea5-6672a4f78172)
- [FDA Inspection 1267173 - 2025-04-18](https://www.globalkeysolutions.net/records/fda_inspections/arboleaf-corporation/30230ae5-554d-4ab7-b8ee-bfa2444714e8)
- [FDA Inspection 1267173 - 2025-04-18](https://www.globalkeysolutions.net/records/fda_inspections/arboleaf-corporation/1d49140e-a0f9-4be9-a0c9-9ae39fe1255b)

Company: https://www.globalkeysolutions.net/companies/arboleaf-corporation/fe88daac-d7f1-4454-8755-e3169086f0da

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