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 3007166613.
Observations1
Issue DateApril 08, 2016
StatusNo Warning Letter
Related Inspections5
Establishment Details
Firm
Octapharma Plasma, Inc.
Location
Newport News, Virginia, United States
FEI Number
3007166613
Product Type
Biologics
Issue Date
April 08, 2016
Country
United States
Inspection History, 2012 to 2020
NAI4
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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