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FDA Inspection 1080179 — Hospira Worldwide, LLC

Hospira Worldwide, LLC — FEI 3005564767

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

Inspection Details

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

Facility

Other inspections at this facility

  • 1299432 (NAI Tue Dec 16 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1037953 (NAI Tue Jan 09 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 830471 (NAI Fri May 03 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 766688 (NAI Wed Jan 18 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 613021 (NAI Fri Sep 18 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources