# FDA Inspection 659230 - Kenneth Yonemura, Md - March 11, 2010

Source: https://www.keypedia.com/records/fda_inspections/kenneth-yonemura-md/c0a7bb13-a1d9-427d-8843-41876bd64ade
Source feed: FDA_Inspections

> FDA Inspection 659230 for Kenneth Yonemura, Md on March 11, 2010. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 659230
- Company Name: Kenneth Yonemura, Md
- Inspection Date: 2010-03-11
- Classification: Official Action Indicated (OAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/kenneth-yonemura-md/d9f1b2cb-1f40-4faa-80e5-1b0623fec647

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