# FDA Inspection 955935 - Riken Keiki Co., Ltd. - December 09, 2015

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

> FDA Inspection 955935 for Riken Keiki Co., Ltd. on December 09, 2015. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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