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Following the closeout, the FDA inspected the pharmacy again from September 13 to September 24, 2021, this time at the Fort Lauderdale location, and issued a Form FDA 483 citing poor sterile practices, referring the matter to the Florida State Board of Pharmacy for follow-up
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![Structure of [ 3 H]liraglutide (top) and the GLP-1 receptor agonists](https://www.researchgate.net/profile/Inga-Bjornsdottir-2/publication/45650716/figure/fig2/AS:667822585806848@1536232720030/Structure-of-3-Hliraglutide-top-and-the-GLP-1-receptor-agonists-liraglutide-and.png)
