Hi all. If we have a supplier that does not make the product (ex. receives product in bead form and grinds into powder form), do we only need to conduct risk assessment for the supplier (i.e. ensure metal from grinder is controlled for) and assume that they have conducted their own assessment, or would we need to seek out documentation about the original manufacture to uncover and control for other risks (i.e. chemical, micro)? Please provide any links from the FDA regarding our responsibility here.
Thanks!