Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1720702.
Observations3
Issue DateAugust 08, 2012
StatusNo Warning Letter
Related Inspections8
Establishment Details
Firm
KEDPlasma LLC
Location
Lincoln, Nebraska, United States
FEI Number
1720702
Product Type
Biologics
Issue Date
August 08, 2012
Country
United States
Inspection History, 2010 to 2025
NAI7
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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