# Riken Keiki Co., Ltd. – FDA Inspection, Jan 30, 2025

Source: https://www.keypedia.com/records/fda_inspections/riken-keiki-co-ltd/689560c1-1ffd-410c-909e-15a77e855eae
Source feed: FDA_Inspections

> FDA inspection 1259495 of Riken Keiki Co., Ltd., January 30, 2025. Classification: Official Action Indicated (OAI). 8 citations under 21 CFR parts 803, 820 and 830. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1259495
- Company Name: Riken Keiki Co., Ltd.
- Inspection Date: 2025-01-30
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 8

## Related Documents

- [FDA Inspection 955935 - 2015-12-09](https://www.keypedia.com/records/fda_inspections/riken-keiki-co-ltd/dfafb81a-4afe-4226-97c3-08d1851968fb)

## Related Officers

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

Company: https://www.keypedia.com/companies/riken-keiki-co-ltd/6cb32b29-e37a-42e2-a8fb-ed171c711836

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8