Filing this as a complaint and a question. The COA I received by email references batch identifier ending in 7-something, but the code laser-etched on the vial I received ends in a different number. Everything else on the label looks normal.
I'm not naming the vendor yet because I want to give them a chance to respond here first, per the complaint guidelines. What's the right way to handle a batch/COA mismatch? Is this always a red flag or can it be an innocent packing error?