# FDA Inspection 1092889 - Sirtex Germany Manufacturing GmbH - April 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/sirtex-germany-manufacturing-gmbh/24361679-8beb-4751-8760-a041ac7690d7
Source feed: FDA_Inspections

> FDA Inspection 1092889 for Sirtex Germany Manufacturing GmbH on April 25, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1092889
- Company Name: Sirtex Germany Manufacturing GmbH
- Inspection Date: 2019-04-25
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1092889 - 2019-04-25](https://www.keypedia.com/records/fda_inspections/sirtex-germany-manufacturing-gmbh/bfa110ae-dd91-45c9-8ece-83aa83eb2b04)

Company: https://www.keypedia.com/companies/sirtex-germany-manufacturing-gmbh/9ddcb46b-6e72-4a53-8fc0-9de6be47bea7

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