# FDA Inspection 621498 - Bieffe Medital SpA - October 16, 2009

Source: https://www.keypedia.com/records/fda_inspections/bieffe-medital-spa/3944e3e4-a9ae-4efc-a936-e42684da688a
Source feed: FDA_Inspections

> FDA Inspection 621498 for Bieffe Medital SpA on October 16, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 621498
- Company Name: Bieffe Medital SpA
- Inspection Date: 2009-10-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/bieffe-medital-spa/a6b2f058-d687-4e04-bfd3-8b59ed1aeddd

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