# FDA Inspection 1085816 - Sakura Seiki Co., Ltd. Yawata Factory - February 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 for Sakura Seiki Co., Ltd. Yawata Factory on February 15, 2019. Classification: Voluntary Action Indicated (VAI).

---

## 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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1204467 - 2023-03-24](https://www.keypedia.com/records/fda_inspections/sakura-seiki-co-ltd-yawata-factory/eddeff16-83e2-4f28-a1e3-9ab518a90291)

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