# Hospira, Inc. – FDA Inspection, Jan 19, 2010

Source: https://www.keypedia.com/records/fda_inspections/hospira-inc/a86b587d-3897-42cd-88ee-22ff5cebd21a
Source feed: FDA_Inspections

> FDA inspection 639034 of Hospira, Inc., January 19, 2010. Classification: Official Action Indicated (OAI). 6 citations under 21 CFR parts 211 and 820. 12 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 639034
- Company Name: Hospira, Inc.
- Inspection Date: 2010-01-19
- 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: 6

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- [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)
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- 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
