# FDA Inspection 1041358 - Amgen Europe BV - January 11, 2018

Source: https://www.keypedia.com/records/fda_inspections/amgen-europe-bv/71c927c5-14af-4b0b-8b9c-f17966266420
Source feed: FDA_Inspections

> FDA Inspection 1041358 for Amgen Europe BV on January 11, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1041358
- Company Name: Amgen Europe BV
- Inspection Date: 2018-01-11
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1204167 - 2022-05-03](https://www.keypedia.com/records/fda_inspections/amgen-europe-bv/21984314-cf0b-4390-b27b-d5d1d39a2830)

Company: https://www.keypedia.com/companies/amgen-europe-bv/869a9ce4-c741-4aec-b25c-d68d881594a7

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