FDA Inspection 673424 — Hospira Inc

Hospira Inc — FEI 2921482

The FDA completed an inspection of Hospira Inc on Jul 28, 2010 in Morgan Hill, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 28, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Morgan Hill, CA (United States)

Citations

IDCFRDescription
416921 CFR 820.100(a)(7)Identifying relevant info for management review