# FDA Inspection 953622 - Fresenius Hemocare Deutschland GmbH - December 03, 2015

Source: https://www.keypedia.com/records/fda_inspections/fresenius-hemocare-deutschland-gmbh/aa029df1-6679-436e-90ec-d2b8602cbdfe
Source feed: FDA_Inspections

> FDA Inspection 953622 for Fresenius Hemocare Deutschland GmbH on December 03, 2015. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 953622
- Company Name: Fresenius Hemocare Deutschland GmbH
- Inspection Date: 2015-12-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/fresenius-hemocare-deutschland-gmbh/44a609c1-6c64-4761-bfa0-611e682d92d9

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