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483
•Edge Biologicals Inc•November 22, 2024

Edge Biologicals Inc – FDA 483, Nov 22, 2024

Record Details

Edge Biologicals Inc, a manufacturer of In Vitro Diagnostic Devices in Memphis, TN, was cited for significant quality system deficiencies during an FDA inspection. The firm failed to adequately establish procedures for corrective and preventive actions, process validation, finished device acceptance, and complaint handling. These issues led to out-of-specification products, microbial contamination, mislabeled products, and inadequate investigations into product quality concerns.

Company
Edge Biologicals Inc
Inspection date
November 22, 2024
Product type
device
Office
New Orleans District Office
Person
  • Jamie P. Webb
View Company Profile

ID · 5f161c54-e882-4a73-b137-36fba38c5926

Other documents for Edge Biologicals Inc
  • 483 - 2023-04-04April 4, 2023
  • 483 - 2022-04-04April 4, 2022

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