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FDA Inspection 1120492 — KEDPLASMA LLC

KEDPLASMA LLC — FEI 1052135

The FDA completed an inspection of KEDPLASMA LLC on March 12, 2020 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
March 12, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Gainesville, FL (United States)

Facility

Other inspections at this facility

  • 987180 (NAI Thu Sep 15 2016 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