FDA issued a Warning Letter to Hospira, Inc. on 4/12/2010 for a previous inspection.
483 Hospira Mar 2012

483 Hospira Mar 2012

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FDA investigators audited the Hospira - Clayton, NC, United States facility and issued inspectional observations (via FDA 483) on 09 Mar 2012.

Product details

  • Category: Human Drugs
  • Inspection end: 09 Mar 2012
  • Location: Clayton, United States
  • FEI: 1048698
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