# FDA Inspection 950051 - Terumo Medical Corporation - October 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/terumo-medical-corporation/4d393933-8ed0-49ba-903e-7a39b5ada30e
Source feed: FDA_Inspections

> FDA Inspection 950051 for Terumo Medical Corporation on October 23, 2015. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 950051
- Company Name: Terumo Medical Corporation
- Inspection Date: 2015-10-23
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/terumo-medical-corporation/436e47e6-b836-4f48-9dbf-0a2f76c31902

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