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483
•Kem Medical Products Corp•January 15, 2020

Kem Medical Products Corp – FDA 483, Jan 15, 2020

Record Details

Kem Medical Products Corp, a medical device manufacturer in Farmingdale, NY, was cited for two observations during an FDA inspection. The firm failed to maintain written Medical Device Reporting (MDR) procedures, specifically lacking electronic MDR procedures for serious injuries and deaths. Additionally, complaint files were not adequately maintained, as the firm did not use its designated form to document consumer complaints since 2016.

Company
Kem Medical Products Corp
Inspection date
January 15, 2020
Product type
device
Office
Division of Human and Animal Food Operations - East I
Person
  • Kwong P. Lee (investigator)
View Company Profile

ID · d29db142-9f8a-4e62-8980-30c4628a49bc

Other documents for Kem Medical Products Corp
  • 483 - 2022-07-21July 21, 2022

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