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Mississippi Devicemaker Repeated 2012 Violations
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Lack of Audits Critical at Software Company
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Smith & Nephew Failed to Address Complaints
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CareFusion Provides Update on Avea Ventilator Recall
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MDR, Validation Issues Top MicroAire Warning Letter
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Fluid Management Manufacturer Warned Over Unreported Upgrades
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Canadian Devicemaker Can’t Sell in U.S. Due to GMP Violations
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Expert Offers Tips on Designing, Running Good Internal Audits
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Signal Medical Lands Warning Over Unapproved Hip Implants
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Better Health Systems Warned Over Failure to Submit PMA
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Smith & Nephew Warned About Morcellator Quality
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Consistency, GMP Guidance Are Lead Priorities at OCP
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