# Sakura Seiki Co., Ltd. Yawata Factory – FDA Inspection, Feb 15, 2019

Source: https://www.keypedia.com/records/fda_inspections/sakura-seiki-co-ltd-yawata-factory/ad05d24c-d0ad-407d-b76a-3fd644759891
Source feed: FDA_Inspections

> FDA inspection 1085816 of Sakura Seiki Co., Ltd. Yawata Factory, February 15, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1085816
- Company Name: Sakura Seiki Co., Ltd. Yawata Factory
- Inspection Date: 2019-02-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1204467 - 2023-03-24

## Related Officers

- [Joshua J. Silvestri](https://www.keypedia.com/people/joshua-j-silvestri/433e29b3-ce5f-44d2-9984-7a6cb61e1824)

Company: https://www.keypedia.com/companies/sakura-seiki-co-ltd-yawata-factory/f78c53bc-8b50-4df6-91d9-f7ef64b651bf

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