# FDA Inspection 950431 - Hospira, Ltd. - November 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/hospira-ltd/a869a49c-99bd-4eea-a5d0-3f43ee3041f4
Source feed: FDA_Inspections

> FDA Inspection 950431 for Hospira, Ltd. on November 19, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 950431
- Company Name: Hospira, Ltd.
- Inspection Date: 2015-11-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 950431 - 2015-11-19](https://www.keypedia.com/records/fda_inspections/hospira-ltd/7f41bac0-4459-4629-8c19-58433ff98392)
- [FDA Inspection 772744 - 2012-03-02](https://www.keypedia.com/records/fda_inspections/hospira-ltd/61da6faa-6cc8-4810-9476-21b035a4c929)
- [FDA Inspection 591778 - 2009-06-18](https://www.keypedia.com/records/fda_inspections/hospira-ltd/ce680eba-7bda-49b7-b078-49b05359d7f9)
- [FDA Inspection 591778 - 2009-06-18](https://www.keypedia.com/records/fda_inspections/hospira-ltd/bd53548b-1a19-46de-a3b8-0269e9c47788)

Company: https://www.keypedia.com/companies/hospira-ltd/69efc79b-6f5b-4a16-bdef-d1b8efb1ea0c

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