# KANEKA MEDIX CORPORATION KANAGAWA PLANT – FDA Inspection, Jan 30, 2025

Source: https://www.keypedia.com/records/fda_inspections/kaneka-medix-corporation-kanagawa-plant/2306dcff-e956-4857-a9b2-0f417094e3f8
Source feed: FDA_Inspections

> FDA inspection 1259483 of KANEKA MEDIX CORPORATION KANAGAWA PLANT, January 30, 2025. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1259483
- Company Name: KANEKA MEDIX CORPORATION KANAGAWA PLANT
- Inspection Date: 2025-01-30
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 2

## 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-medix-corporation-kanagawa-plant/69de47db-29e6-40a0-9b1f-6929e0b32eda

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