# FDA Inspection 1019450 - bioMerieux Italia SpA - June 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 for bioMerieux Italia SpA on June 15, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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