# FDA Inspection 1067945 - Terumo Europe - July 12, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/terumo-europe/a5dad674-2829-47fe-ac62-f2ad021c0efe
Source feed: FDA_Inspections

> FDA Inspection 1067945 for Terumo Europe on July 12, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1067945
- Company Name: Terumo Europe
- Inspection Date: 2018-07-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/terumo-europe/82b97ea5-3921-4bc8-9755-ff2a2327d8c6

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