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FDA Inspection 1024425 — KEDPlasma, LLC

KEDPlasma, LLC — FEI 1044477

The FDA completed an inspection of KEDPlasma, LLC on August 30, 2017 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
August 30, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mobile, AL (United States)

Facility

Other inspections at this facility

  • 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))
  • 649432 (NAI Thu Jan 21 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources