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 3007507466.
Observations3
Issue DateMay 06, 2010
StatusNo Warning Letter
Related Inspections6
Establishment Details
Firm
Octapharma Plasma, Inc.
Location
Des Moines, Iowa, United States
FEI Number
3007507466
Product Type
Biologics
Issue Date
May 06, 2010
Country
United States
Inspection History, 2010 to 2022
NAI5
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
Talk to a Specialist