# ME Center (Nagaizumi) of Terumo Corp – FDA Inspection, Nov 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/me-center-nagaizumi-of-terumo-corp/974db55c-6ec9-4bb2-97a0-a4ca30f7f25b
Source feed: FDA_Inspections

> FDA inspection 1032159 of ME Center (Nagaizumi) of Terumo Corp, November 02, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1032159
- Company Name: ME Center (Nagaizumi) of Terumo Corp
- Inspection Date: 2017-11-02
- 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: 1

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

Company: https://www.keypedia.com/companies/me-center-nagaizumi-of-terumo-corp/9cf227af-502c-4ccd-969b-a5d2254a201d

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