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Foreign Inspections Rise Nearly 30 Percent, CDRH Data Shows
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Root Cause Analysis for Drugs and Devices
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Florida Transdermal Patch Maker Lands 483 for Testing, Complaint Issues
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Mastering the FDA's Import Rules
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FDA Hits Troy for Process Validation, Supplier Qualification Sloppiness
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MHRA Suspends Sales of Silimed Products Following Inspection
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Hospira Device Plant Receives Form 483 for Infusion Pump Battery Failures
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Validation Failures for Cardiac Designs Result in Warning Letter
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Design Validation, CAPA Failures Land Cepheid 483
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Cane S.p.A Gets Warning Letter Over Infusion Pump Procedures
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Rust-Like Contamination Earns Dental Company a Warning Letter
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Managing the Device Supply Chain: Best Practices
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