Some any problems issue bring up that I need your attention. I am referring to the type of approval procedures for items that display different versions on their main labels. The test report used to be issued based on the item description shown on the commercial invoice attached to the application form. However, the Type of Approval Certificate (TAC) is now issued based on the application itself. But importantly, when submitting the Conformity procedures for TAQs, the problem arises when the main label shows two different models, one with aversion number and one without. It is crucial to avoid mistakes that could lead to disastrous consequences as financial penalties can occur.
What should you do if this issue can happen to you?
