# FDA Inspection 1032159 - ME Center (Nagaizumi) of Terumo Corp - November 02, 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 for ME Center (Nagaizumi) of Terumo Corp on November 02, 2017. Classification: Voluntary Action Indicated (VAI).

---

## 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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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