# FDA Inspection 1259483 - KANEKA MEDIX CORPORATION KANAGAWA PLANT - January 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 for KANEKA MEDIX CORPORATION KANAGAWA PLANT on January 30, 2025. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations

## Related Documents

- [FDA Inspection 1259483 - 2025-01-30](https://www.keypedia.com/records/fda_inspections/kaneka-medix-corporation-kanagawa-plant/a781100d-8356-48d5-a2eb-58b3416a82d9)
- [FDA Inspection 1259483 - 2025-01-30](https://www.keypedia.com/records/fda_inspections/kaneka-medix-corporation-kanagawa-plant/60e70857-2796-4bc3-8a35-3f79c1cfb4e5)
- [FDA Inspection 1259483 - 2025-01-30](https://www.keypedia.com/records/fda_inspections/kaneka-medix-corporation-kanagawa-plant/099efb48-e1db-4eea-96b4-e8199d337e03)

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