# Terumo Corporation Fujinomiya Factory – FDA Inspection, Feb 7, 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 of Terumo Corporation Fujinomiya Factory, February 07, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 211. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1004817
- Company Name: Terumo Corporation Fujinomiya Factory
- Inspection Date: 2017-02-07
- 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: 2

## Related Documents

- [FDA Inspection 1206261 - 2023-05-19](https://www.keypedia.com/records/fda_inspections/terumo-corporation-fujinomiya-factory/ffea153e-044e-4781-af5e-1368ccfe4295)
- [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

## Related Officers

- Issuing Officer

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