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Home » Abbott CAPAs Lack Adequate Documentation, FDA 483 Says

Abbott CAPAs Lack Adequate Documentation, FDA 483 Says

June 29, 2023
Devices Inspections and Audits FDA Enforcement Actions
Abbott’s corrective and preventive action (CAPA) activities and results have not been adequately documented, FDA investigators found during an inspection at the company’s Arecibo, Puerto Rico, location.

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