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483
•Qualgen LLC•September 13, 2018

FDA 483 - Qualgen LLC - September 13, 2018

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Record Details

Qualgen LLC, an outsourcing facility in Edmond, OK, was inspected from August 8 to September 13, 2018, and received nine observations. The inspection revealed significant deficiencies in quality control, aseptic processing, facility maintenance, and laboratory controls, including repeat observations related to investigation failures and facility conditions. These issues indicate a lack of adherence to good manufacturing practices and a potential risk to drug product quality and sterility.

Company
Qualgen LLC
Inspection Date
September 13, 2018
Product Type
Drugs
Office
Dallas District Office
People
  • Margaret M. Annes
  • Lisa Whitt (Cornerstone Brands Inc.)
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ID · 853b74b8-eb52-413e-a6d9-a637735a2e24

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