# FDA Inspection 1000903 - Michi Imamura, MD - January 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/michi-imamura-md/d76f712f-d283-4f46-b863-a6f0675ff659
Source feed: FDA_Inspections

> FDA Inspection 1000903 for Michi Imamura, MD on January 13, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000903
- Company Name: Michi Imamura, MD
- Inspection Date: 2017-01-13
- 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/michi-imamura-md/8603ef79-f8ba-4061-ac1d-12ee15c576fa

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