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UnityPoint Health Des Moines IRB Form 483 Details

Form 483
View FDA's record for this firm
Source: FDA inspection recordConfirmed 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 this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3000717839.

UnityPoint Health Des Moines IRB

Des Moines, Iowa, United States
Issue DateMay 19, 2011
FEI Number3000717839
CountryUnited States
Status
No Warning Letter
Product Type
Devices
UnityPoint Health Des Moines IRB FDA Form 483, Des Moines, Iowa, May 19, 2011