# OLYMPUS TERUMO BIOMATERIALS CORP. MISHIMA FACTORY – FDA Inspection, Oct 15, 2009

Source: https://www.keypedia.com/records/fda_inspections/olympus-terumo-biomaterials-corp-mishima-factory/1433560f-5122-410e-b7d3-5fcc6546cb75
Source feed: FDA_Inspections

> FDA inspection 629863 of OLYMPUS TERUMO BIOMATERIALS CORP. MISHIMA FACTORY, October 15, 2009. Classification: Official Action Indicated (OAI). 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 629863
- Company Name: OLYMPUS TERUMO BIOMATERIALS CORP. MISHIMA FACTORY
- Inspection Date: 2009-10-15
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1039108 - 2017-08-25](https://www.keypedia.com/records/fda_inspections/olympus-terumo-biomaterials-corp-mishima-factory/179cca36-f63b-4b0f-89ca-35b7ed648992)

Company: https://www.keypedia.com/companies/olympus-terumo-biomaterials-corp-mishima-factory/1cb3ad20-d57e-45a2-b935-e9ecbdd86691

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