# Mikasa X-Ray Co., Ltd. – FDA Inspection, Jun 5, 2025

Source: https://www.keypedia.com/records/fda_inspections/mikasa-x-ray-co-ltd/a1c48499-a97a-45c9-ad3c-693018969b1d
Source feed: FDA_Inspections

> FDA inspection 1272319 of Mikasa X-Ray Co., Ltd., June 05, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 2

## Related Documents

- [FDA Inspection 1008403 - 2017-03-10](https://www.keypedia.com/records/fda_inspections/mikasa-x-ray-co-ltd/f986d49d-905c-499d-9b87-5d5d29c97118)

## Related Officers

- [Investigator](https://www.keypedia.com/people/preston-m-lee/e44adac3-a915-4bfb-8b06-a41ea5803358)

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

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