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Other FDA-publicized inspection reports of acetaminophen-manufacturing facilities have listed inadequate quality controls, lack of safeguards to isolate rejected raw materials and other drugs, and several human errors resulting in product mix-ups
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This page is a literature-context overview of time-course data reported in the published in-vitro and rodent-model record
Ma Y, Peng D, Liu C, Huang C, Luo J
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