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 3000717839.
Observations1
Issue DateMay 19, 2011
StatusNo Warning Letter
Related Inspections3
Establishment Details
Firm
UnityPoint Health Des Moines IRB
Location
Des Moines, Iowa, United States
FEI Number
3000717839
Product Type
Devices
Issue Date
May 19, 2011
Country
United States
Inspection History, 2011 to 2022
NAI1
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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