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483
•Radix Laboratories Inc•July 25, 2019

Radix Laboratories Inc – FDA 483, Jul 25, 2019

Record Details

Radix Laboratories Inc, an animal drug manufacturer in Eau Claire, WI, was cited for significant deficiencies during an FDA inspection. Observations included releasing drug products before complete testing, failing to follow procedures to prevent objectionable microorganisms in non-sterile products, and inadequate quality control unit procedures regarding document control. These issues indicate a lack of adherence to quality assurance and manufacturing process controls.

Company
Radix Laboratories Inc
Inspection date
July 25, 2019
Product type
veterinary
Office
Minneapolis District Office
Person
  • James K. Ireland (Deputy Commissioner for Foods)
View Company Profile

ID · d0e62ba8-a3ed-4710-b3c4-53719321cbb7

Other documents for Radix Laboratories Inc
  • 483 - 2025-06-27June 27, 2025

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