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FDA Inspection 677221 — KEDPLASMA LLC

KEDPLASMA LLC — FEI 1000135957

The FDA completed an inspection of KEDPLASMA LLC on August 19, 2010 in Bowling Green, KY. 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 19, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bowling Green, KY (United States)

Facility

Other inspections at this facility

  • 1100798 (NAI Wed Jul 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1024406 (NAI Fri Aug 25 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 887854 (NAI Wed Jul 16 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 795633 (NAI Wed Aug 15 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources