FDA issued a Warning Letter to Hospira, Inc. on 4/12/2010 as a result of this inspection.
FDA investigators audited the Hospira - Clayton, NC, United States facility and issued inspectional observations (via FDA 483) on 23 Feb 2010.
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- Category: Animal Drugs & Feeds / Human Drugs / Medical Devices & Rad Health
- Inspection end: 23 Feb 2010
- Location: Clayton, United States
- FEI: 1048698