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FDA Inspection 987180 — KEDPLASMA LLC

KEDPLASMA LLC — FEI 1052135

The FDA completed an inspection of KEDPLASMA LLC on September 15, 2016 in Gainesville, FL. 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
September 15, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Gainesville, FL (United States)

Facility

Other inspections at this facility

  • 1120492 (NAI Thu Mar 12 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 843951 (NAI Wed Aug 14 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 740957 (NAI Wed Aug 24 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources