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FDA Inspection 655221 — KEDPlasma, LLC

KEDPlasma, LLC — FEI 1071645

The FDA completed an inspection of KEDPlasma, LLC on April 2, 2010 in Pensacola, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 2, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pensacola, FL (United States)

Facility

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  • 794796 (NAI Fri Aug 03 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources