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483
•Globus Medical, Inc.•March 28, 2024

FDA 483 - Globus Medical, Inc. - March 28, 2024

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Record Details

An FDA inspection of Globus Medical, Inc. in Methuen, MA, a medical device manufacturer, revealed a significant quality system issue. The firm's device history records for its Excelsius 3D and Excelsius GPS products failed to include required x-ray and laser safety labeling, respectively. This indicates a lack of adherence to manufacturing requirements under 21 CFR 820.

Company
Globus Medical, Inc.
Inspection Date
March 28, 2024
Product Type
Device
Office
New England District Office
Person
  • Nabil Nakhoul
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ID · 879c3eca-3bbe-4ef2-9c0b-efc04ebfb643

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