# FDA Inspection 1276102 - Areka - July 17, 2025

Source: https://www.keypedia.com/records/fda_inspections/areka/f2a6ab54-f5db-411c-a0d6-79b1dc1a3415
Source feed: FDA_Inspections

> FDA Inspection 1276102 for Areka on July 17, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276102
- Company Name: Areka
- Inspection Date: 2025-07-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 963714 - 2016-02-22](https://www.keypedia.com/records/fda_inspections/areka/4a8baf66-0389-4e92-b292-9fecd79cc289)
- [FDA Inspection 963714 - 2016-02-22](https://www.keypedia.com/records/fda_inspections/areka/55540cd5-deed-4256-8840-940ff424ebc2)

Company: https://www.keypedia.com/companies/areka/3d08a65b-9c8a-42bd-bd9c-5d4716cad241

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