FDA Inspection
Kenneth Yonemura, MdKenneth Yonemura, Md – FDA Inspection, Mar 11, 2010
Record Details
This FDA Inspection record concerns Kenneth Yonemura, Md, with an inspection on March 11, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Kenneth Yonemura, Md
- Inspection Date
- March 11, 2010
- Product Type
- Devices
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ID · c0a7bb13-a1d9-427d-8843-41876bd64ade
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 659230
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)(ii)Investigator records of relevant observations inadequate
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