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using it in people, or selling it while implying a therapeutic or muscle-building benefit, can trigger FDA enforcement action against the seller
The general procedure followed in the laboratory for this type includes reconstitution with bacteriostatic or sterile water, storage of the lyophilized powder under cool and dark conditions, and storing the reconstituted solution under cold temperatures to avoid repetitive freeze-thaw cycles and light
Real performance might not match the label
I am hoping someone might cast an eye over the schematic and perhaps advise any glaring or even subtle problems they might see and I should address before I have the board manufactured