# FDA Inspection 584951 - Hospira Inc - May 22, 2009

Source: https://www.keypedia.com/records/fda_inspections/hospira-inc/bf27d4c9-084e-4e6f-b6ee-f7806446bb83
Source feed: FDA_Inspections

> FDA Inspection 584951 for Hospira Inc on May 22, 2009. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 584951
- Company Name: Hospira Inc
- Inspection Date: 2009-05-22
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 673424 - 2010-07-28](https://www.keypedia.com/records/fda_inspections/hospira-inc/c2a36cde-0cff-4fdf-b80d-b590f95ec356)
- [FDA Inspection 673424 - 2010-07-28](https://www.keypedia.com/records/fda_inspections/hospira-inc/8d2d1163-1f15-45a1-aba1-cd78801572ca)
- [FDA Inspection 584951 - 2009-05-22](https://www.keypedia.com/records/fda_inspections/hospira-inc/66343fa9-5eb4-4aeb-9345-9aac7eb2be1e)

Company: https://www.keypedia.com/companies/hospira-inc/bba3d174-1cef-4194-8d0f-67e0fc481022

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