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483
•8046255 Canada Inc.•September 24, 2019

8046255 Canada Inc. – FDA 483, Sep 24, 2019

Record Details

The FDA inspected 8046255 Canada Inc. DBA Viatrexx, a sterile injectable drug product manufacturer in Beloeil, from September 16-24, 2019. The inspection revealed significant deficiencies in aseptic processing, environmental monitoring, laboratory controls, and quality control record-keeping, indicating a severe lack of adherence to cGMP for sterile drug manufacturing. These issues raise serious concerns about the sterility and quality assurance of their injectable drug products.

Company
8046255 Canada Inc.
Inspection date
September 24, 2019
Product type
drugs
Office
Office of Biological Products Operations - Division I
Person
  • Jonathan G. Matrisciano (Program Division Director/District Director)
View Company Profile

ID · 5a6e4438-346a-48c0-9674-280f370ec9c4

Other documents for 8046255 Canada Inc.
  • WARNING_LETTER - 2019-09-24September 24, 2019

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