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483
•Klarity Medical Products LLC•May 20, 2026

Klarity Medical Products LLC – FDA 483, May 20, 2026

Record Details

An FDA inspection of Klarity Medical Products LLC in Heath, OH, revealed four significant observations regarding their quality management system. The firm failed to adequately validate manufacturing processes, monitor supplier performance, verify reworked products, and maintain records of design changes. These issues indicate a lack of robust control over critical aspects of medical device manufacturing and quality assurance.

Company
Klarity Medical Products LLC
Inspection date
May 20, 2026
Product type
device
Office
Cincinnati District Office
Person
  • Javonica F. Penn (investigator)
View Company Profile

ID · f6dd2585-0f29-4135-a3ca-f0e0174d7de0

Other documents for Klarity Medical Products LLC
  • 483 - 2023-02-16February 16, 2023
  • 483 - 2021-07-09July 9, 2021
  • WARNING_LETTER - 2020-02-25February 25, 2020
  • 483 - 2020-02-25February 25, 2020

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