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 3008425048.
Observations2
Issue DateMarch 04, 2015
StatusNo Warning Letter
Related Inspections3
Establishment Details
Firm
Octapharma Plasma Inc
Location
Omaha, Nebraska, United States
FEI Number
3008425048
Product Type
Biologics
Issue Date
March 04, 2015
Country
United States
Inspection History, 2015 to 2018
NAI2
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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