FDA issued a Warning Letter to Hospira, Inc. on 4/12/2010 as a result of this inspection.
483 Hospira Feb 2010

483 Hospira Feb 2010

Thomas Berry FDA, Penny Mccarver FDA, Hai Phung FDA$119.00 - Available Now

FDA investigators audited the Hospira - Clayton, NC, United States facility and issued inspectional observations (via FDA 483) on 23 Feb 2010.

Product details

  • Category: Animal Drugs & Feeds / Human Drugs / Medical Devices & Rad Health
  • Inspection end: 23 Feb 2010
  • Location: Clayton, United States
  • FEI: 1048698
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