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483
•Quadric BioMed, LLC•December 16, 2024

FDA 483 - Quadric BioMed, LLC - December 16, 2024

Record Details

An FDA inspection of Quadric BioMed, LLC, a medical device specification developer in Colorado Springs, CO, revealed significant deficiencies in their quality management system. The firm failed to adequately establish and follow procedures for vendor control, internal quality audits, management reviews, and employee training. These issues indicate a systemic lack of documented processes and records essential for regulatory compliance.

Company
Quadric BioMed, LLC
Inspection date
December 16, 2024
Product type
device
Office
Denver District Office
Person
  • Matthew M. Vernon (investigator)
View Company Profile

ID · b6199e4a-5c34-482a-b3bf-9207fb3269e8

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