# Sakura Seiki Co., Ltd. Chikuma Factory – FDA Inspection, Mar 24, 2023

Source: https://www.keypedia.com/records/fda_inspections/sakura-seiki-co-ltd-chikuma-factory/aff846ed-48ee-47c2-9e32-e93e66855031
Source feed: FDA_Inspections

> FDA inspection 1200617 of Sakura Seiki Co., Ltd. Chikuma Factory, March 24, 2023. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- 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: 8

## Related Documents

- [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 1085815 - 2019-02-15](https://www.keypedia.com/records/fda_inspections/sakura-seiki-co-ltd-chikuma-factory/669b17b0-4f0d-4557-972c-68de59f08249)

## Related Officers

- [Melanie W. Pishnery](https://www.keypedia.com/people/melanie-w-pishnery/ff4846b0-ffe1-4df0-9116-4bb238866b3a)

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