# FDA Inspection 925969 - Fresenius Kabi AB - March 20, 2015

Source: https://www.keypedia.com/records/fda_inspections/fresenius-kabi-ab/a3e711ff-d87c-4235-9d61-c51c4213f150
Source feed: FDA_Inspections

> FDA Inspection 925969 for Fresenius Kabi AB on March 20, 2015. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 925969
- Company Name: Fresenius Kabi AB
- Inspection Date: 2015-03-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1238177 - 2023-04-21](https://www.keypedia.com/records/fda_inspections/fresenius-kabi-ab/62f12c1f-563b-493d-97a3-6340f659dc0d)
- [FDA Inspection 1238177 - 2023-04-21](https://www.keypedia.com/records/fda_inspections/fresenius-kabi-ab/3c7b87ab-53d4-465f-98cd-57b28da356b1)
- [FDA Inspection 1155467 - 2020-10-15](https://www.keypedia.com/records/fda_inspections/fresenius-kabi-ab/45da80c9-a7fb-4e26-8319-4272fc3f5f79)
- [FDA Inspection 1099421 - 2018-10-16](https://www.keypedia.com/records/fda_inspections/fresenius-kabi-ab/601d4a6e-431f-4514-affd-3f8945416a3c)
- [FDA Inspection 1005000 - 2017-02-07](https://www.keypedia.com/records/fda_inspections/fresenius-kabi-ab/5335bdf2-a6c2-4615-9a8d-e8c7eb43064f)

Company: https://www.keypedia.com/companies/fresenius-kabi-ab/95acd39b-72be-48a9-aa55-38713a33c8cc

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