# FDA Inspection 959252 - KOFU FACTORY OF TERUMO CORP. - February 05, 2016

Source: https://www.keypedia.com/records/fda_inspections/kofu-factory-of-terumo-corp/54ff217a-8958-4e2d-b301-108fb003019e
Source feed: FDA_Inspections

> FDA Inspection 959252 for KOFU FACTORY OF TERUMO CORP. on February 05, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 959252
- Company Name: KOFU FACTORY OF TERUMO CORP.
- Inspection Date: 2016-02-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/kofu-factory-of-terumo-corp/e0540434-5dcb-4074-851e-f91bd8bfbbf1

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