# FDA Inspection 697990 - Kyocera Medical Corporation - October 07, 2010

Source: https://www.keypedia.com/records/fda_inspections/kyocera-medical-corporation/52bb406b-dd0b-4a7e-ad7b-ace729442ea1
Source feed: FDA_Inspections

> FDA Inspection 697990 for Kyocera Medical Corporation on October 07, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 697990
- Company Name: Kyocera Medical Corporation
- Inspection Date: 2010-10-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 871691 - 2014-02-28](https://www.keypedia.com/records/fda_inspections/kyocera-medical-corporation/017a1f1f-9820-46c1-b36a-188d9cec5244)
- [FDA Inspection 871691 - 2014-02-28](https://www.keypedia.com/records/fda_inspections/kyocera-medical-corporation/5fa7e64e-7288-46ea-921b-26d9568297e3)
- [FDA Inspection 697990 - 2010-10-07](https://www.keypedia.com/records/fda_inspections/kyocera-medical-corporation/22a732f6-315e-41ad-9076-93c5eaad5279)

Company: https://www.keypedia.com/companies/kyocera-medical-corporation/1b318c41-2365-4dae-b68b-dc256b7e4c9e

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