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FDA Inspection 649432 — KEDPlasma, LLC

KEDPlasma, LLC — FEI 1044477

The FDA completed an inspection of KEDPlasma, LLC on January 21, 2010 in Mobile, AL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 21, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mobile, AL (United States)

Facility

Other inspections at this facility

  • 1024425 (NAI Wed Aug 30 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919447 (NAI Thu Mar 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 841207 (NAI Tue Jul 23 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 657771 (NAI Fri Apr 02 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources