# Areka – FDA Inspection, Jul 17, 2025

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

> FDA inspection 1276102 of Areka, July 17, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 963714 - 2016-02-22

## Related Officers

- [Company Rep](https://www.keypedia.com/people/emily-c-caldwell/101868aa-0586-4d37-8bc6-194f43d66cb7)

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