# Hospira, Inc. – FDA Inspection, Nov 15, 2013

Source: https://www.keypedia.com/records/fda_inspections/hospira-inc/e5c9bb40-43fb-4ad5-a8b3-642e0ff86d62
Source feed: FDA_Inspections

> FDA inspection 855618 of Hospira, Inc., November 15, 2013. Classification: Official Action Indicated (OAI). 12 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 855618
- Company Name: Hospira, Inc.
- Inspection Date: 2013-11-15
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1251941 - 2025-02-07
- [FDA Inspection 1223090 - 2023-11-14](https://www.keypedia.com/records/fda_inspections/hospira-inc/f035aae9-e0b2-49a1-a514-e54edbf04704)
- [FDA Inspection 1110899 - 2019-11-21](https://www.keypedia.com/records/fda_inspections/hospira-inc/8bc1ca51-7f35-4184-ac20-80876c3d27fd)
- [FDA Inspection 1039547 - 2018-02-02](https://www.keypedia.com/records/fda_inspections/hospira-inc/ff0a477b-a209-46bc-a7b5-cd6391330701)
- FDA Inspection 984874 - 2016-05-26

Company: https://www.keypedia.com/companies/hospira-inc/d4decc1e-4b42-43bb-be2c-abcefbc7b965

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