# FDA Inspection 847650 - Terumo Medical Corporation - September 12, 2013

Source: https://www.keypedia.com/records/fda_inspections/terumo-medical-corporation/9ef7a6d5-2da3-45ed-9b4b-a14206346436
Source feed: FDA_Inspections

> FDA Inspection 847650 for Terumo Medical Corporation on September 12, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 847650
- Company Name: Terumo Medical Corporation
- Inspection Date: 2013-09-12
- Classification: No Action Indicated (NAI)
- 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