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Home » FDA Raps OTC Drugmaker for Lax Testing and Maintenance
FDA Raps OTC Drugmaker for Lax Testing and Maintenance
The FDA issued a five-observation Form 483 to Tropical Seas’ over-the-counter drug manufacturing facility in Holly Hill, Fla., for inadequate testing and equipment maintenance, among other lapses observed in a July 11-15 inspection — including several repeat observations from a 2019 warning letter.
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