# FDA Inspection 1095219 - Eurobio Scientific - June 27, 2019

Source: https://www.keypedia.com/records/fda_inspections/eurobio-scientific/141384ce-2eeb-4908-a4e2-b19479d3804f
Source feed: FDA_Inspections

> FDA Inspection 1095219 for Eurobio Scientific on June 27, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095219
- Company Name: Eurobio Scientific
- Inspection Date: 2019-06-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1095219 - 2019-06-27](https://www.keypedia.com/records/fda_inspections/eurobio-scientific/a2d4cd2f-319d-4c00-9ab5-bfac1f29be98)

Company: https://www.keypedia.com/companies/eurobio-scientific/9340bc94-2252-4236-aa48-04ce024f99f2

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