# Kaneka Corporation – FDA Inspection, Apr 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/kaneka-corporation/db652a43-7e4f-4a25-9a8c-13d9bfa40c1a
Source feed: FDA_Inspections

> FDA inspection 1012619 of Kaneka Corporation, April 19, 2017. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1012619
- Company Name: Kaneka Corporation
- Inspection Date: 2017-04-19
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1260082 - 2025-02-06](https://www.keypedia.com/records/fda_inspections/kaneka-corporation/9358167c-d586-4ba9-89ee-781a18a035cb)
- FDA Inspection 962212 - 2016-03-03
- FDA Inspection 800241 - 2012-09-13

## Related Officers

- [Company Rep](https://www.keypedia.com/people/janet-b-abt/e9d87d62-4859-4d36-80c3-c911292349bd)

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

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