# Kaneka Corporation – FDA Inspection, Feb 6, 2025

Source: https://www.keypedia.com/records/fda_inspections/kaneka-corporation/9358167c-d586-4ba9-89ee-781a18a035cb
Source feed: FDA_Inspections

> FDA inspection 1260082 of Kaneka Corporation, February 06, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1260082
- Company Name: Kaneka Corporation
- Inspection Date: 2025-02-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 2

## Related Documents

- [FDA Inspection 1012619 - 2017-04-19](https://www.keypedia.com/records/fda_inspections/kaneka-corporation/db652a43-7e4f-4a25-9a8c-13d9bfa40c1a)
- FDA Inspection 962212 - 2016-03-03
- FDA Inspection 800241 - 2012-09-13

## Related Officers

- [Dianiris C. Ayala](https://www.keypedia.com/people/dianiris-c-ayala/ba6c5538-201b-4c9a-8f23-e160db6868e6)

Company: https://www.keypedia.com/companies/kaneka-corporation/3f38f4de-3d78-415b-91d6-945a7bee153f

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8