What strikes me most is the insane amount of CLUTTER.
It's not just a little bit, it's enough that it HAS to inhibit the workers / product. Absolutely nothing is organized (maybe your masteron that ended up being test wasn't due to the supplier scamming you, maybe it's just because they ran such a shit practice and didn't know what they were putting into the products--but I digress).
Also...if people only knew the insane standards it takes to meet USP guidelines for sterile compounding (these are enforceable by the FDA in the US), they'd just always assume that NO lab, whether they claim pharma or not (unless it's a real one, i.e. bayer, schering, etc) outside the US even remotely meets these guidelines.
The amount of regulation / sanitation / practices you have to follow in sterile compounding is insane. I'm not saying that a decent product can't be produced outside these conditions, but I am saying that it's nowhere close to USP / GMP quality, that's for sure.