# Riken Keiki Co., Ltd. – FDA Inspection, Dec 9, 2015

Source: https://www.keypedia.com/records/fda_inspections/riken-keiki-co-ltd/dfafb81a-4afe-4226-97c3-08d1851968fb
Source feed: FDA_Inspections

> FDA inspection 955935 of Riken Keiki Co., Ltd., December 09, 2015. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 955935
- Company Name: Riken Keiki Co., Ltd.
- Inspection Date: 2015-12-09
- 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: 3

## Related Documents

- [FDA Inspection 1259495 - 2025-01-30](https://www.keypedia.com/records/fda_inspections/riken-keiki-co-ltd/689560c1-1ffd-410c-909e-15a77e855eae)

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

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