# FDA Inspection 1073224 - Ashitaka Factory of Terumo Corporation - October 31, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/ashitaka-factory-of-terumo-corporation/3513b049-212a-4f8b-b753-e4814b37b943
Source feed: FDA_Inspections

> FDA Inspection 1073224 for Ashitaka Factory of Terumo Corporation on October 31, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1073224
- Company Name: Ashitaka Factory of Terumo Corporation
- Inspection Date: 2018-10-31
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 923480 - 2015-03-05](https://www.globalkeysolutions.net/records/fda_inspections/ashitaka-factory-of-terumo-corporation/6bc94d41-3c5e-4c23-84fe-4eb36fc45d46)

Company: https://www.globalkeysolutions.net/companies/ashitaka-factory-of-terumo-corporation/dd36ad17-b88f-4dc9-bd2f-d5023ad07845

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