# Terumo Medical Corporation – FDA Inspection, Jan 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/terumo-medical-corporation/9a2c1384-ab67-43d2-8e01-8c3414dafafd
Source feed: FDA_Inspections

> FDA inspection 1003680 of Terumo Medical Corporation, January 13, 2017. Classification: No Action Indicated (NAI). 4 citations under 21 CFR part 820. Form 483 issued. 8 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003680
- Company Name: Terumo Medical Corporation
- Inspection Date: 2017-01-13
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

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- [FDA Inspection 950051 - 2015-10-23](https://www.keypedia.com/records/fda_inspections/terumo-medical-corporation/4d393933-8ed0-49ba-903e-7a39b5ada30e)

## Related Officers

- Issuing Officer

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