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A foreign company (that we work with) is requesting a CFG to facilitate registration of their product in Costa Rica. Apparently, Costa Rica is more responsive to FDA's CFG over their country's FSC. I have informed them that the products listed on the CFG would need to be exported from the US. They have informed me that would not be the case, that this document is only going to be used to speed the registration process and once registered, Costa Rica will not have any issue where the product will be coming from. I can see what appears to be a loop hole here, but I refuse to apply for the CFG knowing the product will not be exported from the US.
Has anyone had any experience with this?
Thanks in advance!
Has anyone had any experience with this?
Thanks in advance!
