483
Pharmavite LLC - OpelikaPharmavite LLC - Opelika – FDA 483, Jul 25, 2025
Record Details
Pharmavite LLC - Opelika received a Form FDA 483 following an inspection from July 21-25, 2025. The inspection revealed a significant issue with batch production records, specifically regarding incomplete documentation and premature initialing for critical manufacturing steps. This indicates a lapse in maintaining accurate and complete records for product manufacturing.
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ID · 2a158497-eca3-4ca4-b9b0-70d1ba1ee1de
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