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FDA Inspection 944212 — Kedplasma LLC

Kedplasma LLC — FEI 3004158206

The FDA completed an inspection of Kedplasma LLC on September 30, 2015 in Temple Terrace, 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 30, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Temple Terrace, FL (United States)

Facility

Other inspections at this facility

  • 1295862 (NAI Wed Dec 10 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1032352 (NAI Mon Oct 09 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 830577 (NAI Tue May 07 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 718683 (NAI Fri Apr 08 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 555184 (NAI Thu Jan 08 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources