# FDA Inspection 1194249 - Abiomed Europe GmbH - November 10, 2022

Source: https://www.keypedia.com/records/fda_inspections/abiomed-europe-gmbh/bfcfa064-811e-4921-a306-9a5c3ddf26aa
Source feed: FDA_Inspections

> FDA Inspection 1194249 for Abiomed Europe GmbH on November 10, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1194249
- Company Name: Abiomed Europe GmbH
- Inspection Date: 2022-11-10
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 979231 - 2016-06-23](https://www.keypedia.com/records/fda_inspections/abiomed-europe-gmbh/680fc4e9-e70d-4591-a6b8-fb8104050d8d)
- [FDA Inspection 910065 - 2014-12-18](https://www.keypedia.com/records/fda_inspections/abiomed-europe-gmbh/94804f46-dd21-471d-b14b-bbe20b733f88)

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