# Eurobio Scientific – FDA Inspection, Jun 27, 2019

Source: https://www.keypedia.com/records/fda_inspections/eurobio-scientific/a2d4cd2f-319d-4c00-9ab5-bfac1f29be98
Source feed: FDA_Inspections

> FDA inspection 1095219 of Eurobio Scientific, June 27, 2019. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/kirtida-patel/c62852cf-9724-4296-bc4b-de8993dcf716)

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