FDA Inspection
Kenji Ando, M.D.Kenji Ando, M.D. – FDA Inspection, Oct 31, 2019
Record Details
This FDA Inspection record concerns Kenji Ando, M.D., with an inspection on October 31, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Kenji Ando, M.D.
- Inspection Date
- October 31, 2019
- Product Type
- Devices
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ID · ff8ac8f1-ae48-4605-97b1-e8cf41e6a818
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1110723
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
Other FDA inspections of Kenji Ando, M.D.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 17, 2014 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
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