# Terumo Medical Corporation – FDA Inspection, Jun 20, 2019

Source: https://www.keypedia.com/records/fda_inspections/terumo-medical-corporation/64690c93-12b4-40b1-833d-882ddc9f0d1b
Source feed: FDA_Inspections

> FDA inspection 1094113 of Terumo Medical Corporation, June 20, 2019. Classification: Voluntary Action Indicated (VAI). 3 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: 1094113
- Company Name: Terumo Medical Corporation
- Inspection Date: 2019-06-20
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

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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

- [Company Rep](https://www.keypedia.com/people/daniel-t-lee/8147e5b2-2065-42e3-b86c-36c0231f74cc)
- [Issuing Officer](https://www.keypedia.com/people/jacob-m-dyer/e3ca27e3-e0b1-4db8-9cbe-cfaff90b83cf)

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