# FDA Inspection 979231 - Abiomed Europe GmbH - June 23, 2016

Source: https://www.keypedia.com/records/fda_inspections/abiomed-europe-gmbh/680fc4e9-e70d-4591-a6b8-fb8104050d8d
Source feed: FDA_Inspections

> FDA Inspection 979231 for Abiomed Europe GmbH on June 23, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 979231
- Company Name: Abiomed Europe GmbH
- Inspection Date: 2016-06-23
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/abiomed-europe-gmbh/3e14804c-6f1d-41b8-84a0-f1c6ff374174

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