DashboardForm 483sForm 483 Details

Kansas City Oncology Program 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 3009197681.

Kansas City Oncology Program IRB

Prairie Village, Kansas, United States
Issue DateJanuary 26, 2012
FEI Number3009197681
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Kansas City Oncology Program IRB FDA Form 483, Prairie Village, Kansas, January 26, 2012