FDA Inspection 1080179 — Hospira Worldwide, LLC

Hospira Worldwide, LLC — FEI 3005564767

The FDA completed an inspection of Hospira Worldwide, LLC on Jan 29, 2019 in Pleasant Prairie, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jan 29, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Pleasant Prairie, WI (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.