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  • The FDA, the then-Canadian Radiation Protection Bureau (CRPB), and the users were informed that there was a problem, although the users claim that they were never informed that a patient injury had occurred. (On April 1, 1986, the CRPB and the Bureau of Medical Devices were merged to form the Bureau of Radiation and Medical Devices or BRMD.) Users were told that they should visually confirm the tu
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