# FDA Inspection 966015 - Sankei Co., Ltd. - April 07, 2016

Source: https://www.keypedia.com/records/fda_inspections/sankei-co-ltd/28256690-c74d-47a0-9b76-d0b85a2b8363
Source feed: FDA_Inspections

> FDA Inspection 966015 for Sankei Co., Ltd. on April 07, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 966015
- Company Name: Sankei Co., Ltd.
- Inspection Date: 2016-04-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/sankei-co-ltd/cb02bbb9-9086-46d1-8338-e3b9dff7ed2f

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