# FDA Inspection 1110723 - Kenji Ando, M.D. - October 31, 2019

Source: https://www.keypedia.com/records/fda_inspections/kenji-ando-md/ff8ac8f1-ae48-4605-97b1-e8cf41e6a818
Source feed: FDA_Inspections

> FDA Inspection 1110723 for Kenji Ando, M.D. on October 31, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1110723
- Company Name: Kenji Ando, M.D.
- Inspection Date: 2019-10-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 893786 - 2014-07-17](https://www.keypedia.com/records/fda_inspections/kenji-ando-md/4a086663-55c3-42e6-aaba-75b1b5120595)

Company: https://www.keypedia.com/companies/kenji-ando-md/e8c58c78-4ae5-42ae-be2b-bfd3b9562f3f

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