Summary - Revision of Violation Examples Involving Medical Use of Byproduct Material

On April 24, 2002, the Commission published a revision to the Enforcement Policy in the Federal Register (67 FR 20187) revising examples of severity levels for violations associated with the requirements to use written directives for certain medical uses of byproduct material; and to develop, implement, and maintain uses that require a written directive (10 CFR 35.40 and 35.41). These examples are used to provide guidance for determining the significance of a particular violation.