# FDA Inspection 947824 - Kyowa Seiko Co Ltd - October 08, 2015

Source: https://www.keypedia.com/records/fda_inspections/kyowa-seiko-co-ltd/7cde75f1-76fe-4f6b-98b3-65e6e94f6986
Source feed: FDA_Inspections

> FDA Inspection 947824 for Kyowa Seiko Co Ltd on October 08, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 947824
- Company Name: Kyowa Seiko Co Ltd
- Inspection Date: 2015-10-08
- 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/kyowa-seiko-co-ltd/6683be78-18b3-4253-82e3-89e79c645383

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