FDA 483 - Natureplex LLC - July 24, 2025
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Natureplex LLC, a drug manufacturer in Olive Branch, MS, received a Form 483 citing significant deficiencies in its quality control unit and investigation procedures. The inspection revealed inadequate laboratory investigations, unaddressed consumer complaints, and insufficient stability studies, indicating a failure to ensure drug products meet cGMP standards for safety, efficacy, purity, and quality. These issues highlight a systemic lack of oversight and thoroughness in quality management processes.
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