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Home » Medtronic Diabetes receives FDA warning over quality system requirement inadequacies

Medtronic Diabetes receives FDA warning over quality system requirement inadequacies

December 15, 2021 By Sean Whooley

MedtronicMedtronic (NYSE:MDT) announced today that it received an FDA warning letter after an inspection of its Diabetes Business.

The company received the letter on Dec. 9 for its Northridge, California facility — the Medtronic Diabetes Business headquarters — following an inspection that concluded in July 2021.

Shares of MDT were down 6.3% at $104.62 per share in early-morning trading today on the back of the news of the FDA letter. The company’s shares finished the day down 6% in total at $104.94 per share.

Get the full story at our sister site, Drug Delivery Business News.

Filed Under: Business/Financial News, Diabetes, Drug Pumps, Drug-Device Combinations, Featured, Food & Drug Administration (FDA), News Well, Recalls, Regulatory/Compliance Tagged With: FDA, Medtronic

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About Sean Whooley

Sean Whooley is a senior editor who mainly produces work for MassDevice, Medical Design & Outsourcing and Drug Delivery Business News. He received a bachelor's degree in multiplatform journalism from the University of Maryland, College Park. You can connect with him on LinkedIn or email him at [email protected].

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