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483
•PhytogenX, Inc.•February 10, 2020

PhytogenX, Inc. – FDA 483, Feb 10, 2020

Record Details

An FDA inspection of PhytogenX, Inc., a drug manufacturer in Morgantown, PA, revealed significant deficiencies across multiple areas. Observations included failures in following and documenting established laboratory control mechanisms and test procedures, inadequate investigation of unexplained discrepancies, and a lack of adherence to written quality control unit responsibilities and procedures, including several Standard Operating Procedures.

Company
PhytogenX, Inc.
Inspection date
February 10, 2020
Product type
drugs
Office
Philadelphia District Office
People
  • Christina K. Theodorou (Consumer Safety Officer)
  • Rachael O. Oyewole
View Company Profile

ID · 74b6f0a2-88b8-4648-b026-feb4ae03a1e9

Other documents for PhytogenX, Inc.
  • 483 - 2025-03-27March 27, 2025
  • 483 - 2019-02-14February 14, 2019

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