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Home » Heany Industries Gets Form 483 for Inadequate Validations, CAPAs
Heany Industries Gets Form 483 for Inadequate Validations, CAPAs
The FDA hit Heany Industries, a manufacturer of industrial ceramics and thermally based coatings, with a Form 483 for inadequate validations and corrective and preventive action (CAPA) procedures after an inspection of its Scottsville, N.Y., facility in March.