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483
•Continental Manufacturing Chemist•May 10, 2023

Continental Manufacturing Chemist – FDA 483, May 10, 2023

Record Details

Continental Manufacturing Chemist, an OTC manufacturer in Huxley, IA, was cited for significant quality control deficiencies during an FDA inspection. Observations included inadequate component testing for impurities, failure to validate supplier analyses, and lack of appropriate controls over computer systems and production records. Additionally, the firm failed to follow written procedures for equipment cleaning and maintenance, leading to visible residue on manufacturing vessels.

Company
Continental Manufacturing Chemist
Inspection date
May 10, 2023
Product type
drugs
Office
Division of Human and Animal Food Operations - West II
Person
  • Torrey M. Ward
View Company Profile

ID · 90af2145-ad80-4340-9e6f-071ef22a9c11

Other documents for Continental Manufacturing Chemist
  • 483 - 2019-07-30July 30, 2019

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