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 3006604254.
Observations3
Issue DateJanuary 08, 2015
StatusNo Warning Letter
Related Inspections6
Establishment Details
Firm
Octapharma Plasma Inc
Location
Omaha, Nebraska, United States
FEI Number
3006604254
Product Type
Biologics
Issue Date
January 08, 2015
Country
United States
Inspection History, 2009 to 2021
NAI4
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.