# FDA Inspection 1200617 - Sakura Seiki Co., Ltd. Chikuma Factory - March 24, 2023

Source: https://www.keypedia.com/records/fda_inspections/sakura-seiki-co-ltd-chikuma-factory/638ce009-49fd-4640-9d7a-691c0d1a76ff
Source feed: FDA_Inspections

> FDA Inspection 1200617 for Sakura Seiki Co., Ltd. Chikuma Factory on March 24, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1200617
- Company Name: Sakura Seiki Co., Ltd. Chikuma Factory
- Inspection Date: 2023-03-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1311276 - 2026-03-05](https://www.keypedia.com/records/fda_inspections/sakura-seiki-co-ltd-chikuma-factory/9435149e-3c23-4bb4-9fe3-4ce64d480615)
- [FDA Inspection 1200617 - 2023-03-24](https://www.keypedia.com/records/fda_inspections/sakura-seiki-co-ltd-chikuma-factory/aff846ed-48ee-47c2-9e32-e93e66855031)

Company: https://www.keypedia.com/companies/sakura-seiki-co-ltd-chikuma-factory/f9b79c21-3fd4-4ff7-bdd8-a97c13aa71e2

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