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 1377602.
Observations6
Issue DateDecember 05, 2012
StatusNo Warning Letter
Related Inspections6
Establishment Details
Firm
KEDPlasma LLC
Location
Williamsville, New York, United States
FEI Number
1377602
Product Type
Biologics
Issue Date
December 05, 2012
Country
United States
Inspection History, 2011 to 2019
NAI5
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.