# FDA Inspection 884787 - Diasorin Deutschland GmbH - May 30, 2014

Source: https://www.keypedia.com/records/fda_inspections/diasorin-deutschland-gmbh/6f4ecf51-aeb8-46e4-8448-c74a51f9f771
Source feed: FDA_Inspections

> FDA Inspection 884787 for Diasorin Deutschland GmbH on May 30, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 884787
- Company Name: Diasorin Deutschland GmbH
- Inspection Date: 2014-05-30
- 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/diasorin-deutschland-gmbh/a568a5e5-2123-4e66-9b8a-70df2899868e

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