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 3007899522.
Observations1
Issue DateAugust 26, 2013
StatusNo Warning Letter
Related Inspections4
Establishment Details
Firm
Octapharma Plasma, Inc.
Location
Richmond, Virginia, United States
FEI Number
3007899522
Product Type
Biologics
Issue Date
August 26, 2013
Country
United States
Inspection History, 2013 to 2021
NAI3
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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