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Magnolia Medical Announces Successful FDA Field Inspection Results and Formal Warning Letter Close-Out

/PRNewswire/ Magnolia Medical Technologies, Inc., ("Magnolia") inventors of the Steripath® Initial Specimen Diversion Device® (ISDD®), today announced that.

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Magnolia Medical Announces Successful FDA Field Inspection Results and Formal Warning Letter Close-Out

Magnolia Medical Announces Successful FDA Field Inspection Results and Formal Warning Letter Close-Out
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Newly Released CLSI National Blood Culture Guidelines Identify Best Practices and Evidence-Based Technology Solutions Such as Steripath® to Improve Patient Safety and Outcomes

/PRNewswire/ Magnolia Medical Technologies, Inc., commends Clinical Laboratory Standards Institute (CLSI) for establishing a goal of 1% blood culture.

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Magnolia Medical, MHA Solutions, and Healthcare Providers Insurance Company Enter into an Exclusive, Endorsed Agreement for the Steripath® Initial Specimen Diversion Device®

/PRNewswire/ Magnolia Medical Technologies, Inc., inventors of Steripath®, the only FDA 510(k)-cleared device platform indicated to reduce blood culture.

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Members of Congress Urge CMS to Take Action to Reduce Preventable False-Positive Diagnostic Test Results for Sepsis

/PRNewswire/ Magnolia Medical Technologies, Inc., inventors of Steripath®, the only FDA 510(k)-cleared device platform indicated to reduce blood culture.

United statesGus bilirakisMike levinClin microbiolGreg bullingtonForum infect disUs department of healthVeterans affairsMagnolia medical technologies incHuman servicesCenters for medicareDepartment of veterans affairsMedicaid servicesMagnolia medical technologiesRepresentative gusRepresentatives levin