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483
•Johnson Medtech LLC•November 27, 2023

Johnson Medtech LLC – FDA 483, Nov 27, 2023

Record Details

Johnson Medtech LLC, a medical device manufacturer in Vandalia, OH, received a Form FDA 483 with four repeat observations. The inspection revealed significant deficiencies in process validation, production process control, corrective and preventive action procedures, and product acceptance status. These issues indicate a systemic lack of adherence to quality system requirements, posing potential risks to device quality and patient safety.

Company
Johnson Medtech LLC
Inspection date
November 27, 2023
Product type
device
Office
Cincinnati District Office
Person
  • Rosanna M. Goodrich (Medical Device Specialist)
View Company Profile

ID · a1a30be7-8fb4-4b8a-8360-f9d2bfa09d70

Other documents for Johnson Medtech LLC
  • 483 - 2022-12-08December 8, 2022
  • 483 - 2019-06-06June 6, 2019

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