# bioMerieux Italia SpA – FDA Inspection, Jun 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/biomerieux-italia-spa/f48beff7-094c-434a-9970-840ba8d63037
Source feed: FDA_Inspections

> FDA inspection 1019450 of bioMerieux Italia SpA, June 15, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1019450
- Company Name: bioMerieux Italia SpA
- Inspection Date: 2017-06-15
- 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: 0

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

Company: https://www.keypedia.com/companies/biomerieux-italia-spa/0fca498f-dafd-49b2-b72e-b72b3b0d12fe

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