# FDA Inspection 1259483 - KANEKA MEDIX CORPORATION KANAGAWA PLANT - January 30, 2025

Source: https://www.keypedia.com/records/fda_inspections/kaneka-medix-corporation-kanagawa-plant/099efb48-e1db-4eea-96b4-e8199d337e03
Source feed: FDA_Inspections

> FDA Inspection 1259483 for KANEKA MEDIX CORPORATION KANAGAWA PLANT on January 30, 2025. Classification: Voluntary Action Indicated (VAI).

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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: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1259483 - 2025-01-30](https://www.keypedia.com/records/fda_inspections/kaneka-medix-corporation-kanagawa-plant/2306dcff-e956-4857-a9b2-0f417094e3f8)
- [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)

Company: https://www.keypedia.com/companies/kaneka-medix-corporation-kanagawa-plant/69de47db-29e6-40a0-9b1f-6929e0b32eda

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