# Sivantos GmbH – FDA Inspection, Oct 31, 2013

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

> FDA inspection 857143 of Sivantos GmbH, October 31, 2013. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803, 806 and 820. 2 other FDA inspections on record for this company.

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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)
- 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: 5

## Related Documents

- [FDA Inspection 1196667 - 2023-02-02](https://www.keypedia.com/records/fda_inspections/sivantos-gmbh/ef78ec40-bada-45d0-816d-a9cff79e7289)
- FDA Inspection 1079959 - 2018-05-17

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