# FDA Inspection 1272319 - Mikasa X-Ray Co., Ltd. - June 05, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/mikasa-x-ray-co-ltd/5520b5f4-54cd-43f4-b9ec-ae786ed35414
Source feed: FDA_Inspections

> FDA Inspection 1272319 for Mikasa X-Ray Co., Ltd. on June 05, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1272319
- Company Name: Mikasa X-Ray Co., Ltd.
- Inspection Date: 2025-06-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1272319 - 2025-06-05](https://www.globalkeysolutions.net/records/fda_inspections/mikasa-x-ray-co-ltd/a1c48499-a97a-45c9-ad3c-693018969b1d)
- [FDA Inspection 1272319 - 2025-06-05](https://www.globalkeysolutions.net/records/fda_inspections/mikasa-x-ray-co-ltd/7607ae75-9e5f-4c18-9bb2-8f2f1c138bb8)
- [FDA Inspection 1272319 - 2025-06-05](https://www.globalkeysolutions.net/records/fda_inspections/mikasa-x-ray-co-ltd/1ac17450-f092-44bc-974b-f15e6f302b57)
- [FDA Inspection 1008403 - 2017-03-10](https://www.globalkeysolutions.net/records/fda_inspections/mikasa-x-ray-co-ltd/de7e00e2-2de4-4b3e-963c-6578103a193d)
- [FDA Inspection 1008403 - 2017-03-10](https://www.globalkeysolutions.net/records/fda_inspections/mikasa-x-ray-co-ltd/f986d49d-905c-499d-9b87-5d5d29c97118)

Company: https://www.globalkeysolutions.net/companies/mikasa-x-ray-co-ltd/89554b99-2409-4c61-80ed-03a26764d292

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