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483
•Sciegen Pharmaceuticals Inc•January 9, 2015

FDA 483 - Sciegen Pharmaceuticals Inc - January 09, 2015

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Record Details

An FDA inspection of Sciegen Pharmaceuticals Inc. in Hauppauge, NY, revealed that the firm's quality control unit procedures were not fully followed. Specifically, a laboratory investigation into duplicate sample sets for Metformin Hydrochloride Tablets was deemed inadequate. The firm failed to determine the root cause of the event and did not conduct a comprehensive review of electronic files and associated audit trails.

Company
Sciegen Pharmaceuticals Inc
Inspection Date
January 9, 2015
Product Type
Drugs
Office
Division of Human and Animal Food Operations - East I
Person
  • Robert C. Horan (Biotechnology Specialist at FDA)
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ID · 5e31791b-c59c-42d6-8153-31d0bd380825

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