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483
•Haleon US Inc.•September 30, 2021

Haleon US Inc. – FDA 483, Sep 30, 2021

Record Details

An FDA inspection of GSK Consumer Health Inc. in Lincoln, NE, revealed significant deficiencies in quality control and manufacturing processes. The firm failed to thoroughly review out-of-specification materials and packaging defects, leading to distributed products with potential quality issues. Additionally, there were inadequate written procedures for the quality control unit, equipment cleaning, microbial control in water systems, and the drug product stability program.

Company
Haleon US Inc.
Inspection date
September 30, 2021
Product type
drugs
Office
Division of Human and Animal Food Operations - West II
People
  • Jacob G. Lutz (Investigator)
  • Sandra A. Boyd (Drug National Expert)
  • Lisa L. Flores (Consumer Safety Officer/ Federal Investigator)
View Company Profile

ID · 62f851a1-563f-4ffc-a4ec-eb6f8d67e1b3

Other documents for Haleon US Inc.
  • 483 - 2013-02-14February 14, 2013
  • 483 - 2011-07-08July 8, 2011

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