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FDA Inspection 844785 — Hospira, Inc.

Hospira, Inc. — FEI 1925262

The FDA completed an inspection of Hospira, Inc. on August 16, 2013 in Mcpherson, KS. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 16, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mcpherson, KS (United States)

Facility

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Recent compliance actions

FDA data resources