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The allegations center on product quality and sterility standards in compounded GLP-1 medications, with the family asserting the compounded injection differed in safety profile from FDA-approved versions of semaglutide products

Then, we cross-referenced facilities associated with imports of semaglutide, tirzepatide, pembrolizumab, and antibiotics with the FDAs Registered Drug Establishments list using the manufacturer FEI number, the manufacturer name, or the manufacturer address

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