# Mikasa X-Ray Co., Ltd. – FDA Inspection, Mar 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/mikasa-x-ray-co-ltd/f986d49d-905c-499d-9b87-5d5d29c97118
Source feed: FDA_Inspections

> FDA inspection 1008403 of Mikasa X-Ray Co., Ltd., March 10, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1008403
- Company Name: Mikasa X-Ray Co., Ltd.
- Inspection Date: 2017-03-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 1272319 - 2025-06-05](https://www.keypedia.com/records/fda_inspections/mikasa-x-ray-co-ltd/a1c48499-a97a-45c9-ad3c-693018969b1d)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jacqueline-s-warner/d001f4ec-db46-4d78-a5dd-efea7ddfb893)

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

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