# FDA Inspection 857143 - Sivantos GmbH - October 31, 2013

Source: https://www.keypedia.com/records/fda_inspections/sivantos-gmbh/9982a2df-d782-4969-8e2e-b4e68cfda7d9
Source feed: FDA_Inspections

> FDA Inspection 857143 for Sivantos GmbH on October 31, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 857143
- Company Name: Sivantos GmbH
- Inspection Date: 2013-10-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 857143 - 2013-10-31](https://www.keypedia.com/records/fda_inspections/sivantos-gmbh/951ec058-19ac-40fb-864f-ac76f4206b29)

Company: https://www.keypedia.com/companies/sivantos-gmbh/bbdf956b-4050-44c2-99f4-f5c12836cda7

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