# FDA Inspection 1004817 - Terumo Corporation Fujinomiya Factory - February 07, 2017

Source: https://www.keypedia.com/records/fda_inspections/terumo-corporation-fujinomiya-factory/e4ec0ca3-41ef-46be-ab3a-96093ca6bbc7
Source feed: FDA_Inspections

> FDA Inspection 1004817 for Terumo Corporation Fujinomiya Factory on February 07, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1004817
- Company Name: Terumo Corporation Fujinomiya Factory
- Inspection Date: 2017-02-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1004817 - 2017-02-07](https://www.keypedia.com/records/fda_inspections/terumo-corporation-fujinomiya-factory/46759c3a-ffaa-44a7-8b21-f8183a58a7e3)
- [FDA Inspection 875358 - 2014-03-20](https://www.keypedia.com/records/fda_inspections/terumo-corporation-fujinomiya-factory/3f241b1e-852e-4ff9-a67b-5a9d34a7330b)
- [FDA Inspection 746978 - 2011-09-16](https://www.keypedia.com/records/fda_inspections/terumo-corporation-fujinomiya-factory/8b78666d-c3b7-4b8b-9026-7037f8ca8ae1)

Company: https://www.keypedia.com/companies/terumo-corporation-fujinomiya-factory/82a74871-bc83-43dc-b1cc-7ae24148d80f

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