# FDA Inspection 1096452 - Fujirebio Europe N.V. - June 06, 2019

Source: https://www.keypedia.com/records/fda_inspections/fujirebio-europe-nv/05c1265f-7d4e-4a87-bb92-6f89fc00b847
Source feed: FDA_Inspections

> FDA Inspection 1096452 for Fujirebio Europe N.V. on June 06, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1096452
- Company Name: Fujirebio Europe N.V.
- Inspection Date: 2019-06-06
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/fujirebio-europe-nv/996335ef-584f-4ca6-b05c-928c179aa8fe

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