# FDA Inspection 965779 - Kenneth Yamamura, MD - April 11, 2016

Source: https://www.keypedia.com/records/fda_inspections/kenneth-yamamura-md/bfebb622-5b17-4cec-b45e-b47cb1425512
Source feed: FDA_Inspections

> FDA Inspection 965779 for Kenneth Yamamura, MD on April 11, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 965779
- Company Name: Kenneth Yamamura, MD
- Inspection Date: 2016-04-11
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/kenneth-yamamura-md/cef1ca61-cb4f-470b-a9d6-95fd8aa8f936

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