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Home » FDA Inspection Finds Fault with Repaired Philips Respironics Breathing Devices
FDA Inspection Finds Fault with Repaired Philips Respironics Breathing Devices
An FDA inspection of a Philips Respironics facility in Pennsylvania has turned up problems that will delay the company’s replacement of millions of its ventilators, continuous positive airway pressure (CPAP) and bilevel positive airway pressure (BiPAP) machines.