# FDA Inspection 1015135 - Itoh Akinobu - April 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/itoh-akinobu/3f564266-b9fb-4348-b24f-776cd4d9f91b
Source feed: FDA_Inspections

> FDA Inspection 1015135 for Itoh Akinobu on April 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1015135
- Company Name: Itoh Akinobu
- Inspection Date: 2017-04-21
- 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/itoh-akinobu/fdd9d36a-7496-49e9-896d-568bf161e526

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