FDA Inspection
Sakura Seiki Co., Ltd. Yawata FactorySakura Seiki Co., Ltd. Yawata Factory – FDA Inspection, Feb 15, 2019
Record Details
This FDA Inspection record concerns Sakura Seiki Co., Ltd. Yawata Factory, with an inspection on February 15, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · ad05d24c-d0ad-407d-b76a-3fd644759891
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1085816
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Sakura Seiki Co., Ltd. Yawata Factory
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 24, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Sakura Seiki Co., Ltd. Yawata Factory
- FDA Inspection 1204467 - 2023-03-24
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