# FDA Inspection 942202 - Hospira, Inc. - September 24, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/hospira-inc/5ffad654-432c-4279-bb5b-e6ff8854b145/
Source feed: FDA_Inspections

> FDA Inspection 942202 for Hospira, Inc. on September 24, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 942202
- Company Name: Hospira, Inc.
- Inspection Date: 2015-09-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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