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483
•DRF Medical Group Inc•September 24, 2015

FDA 483 - DRF Medical Group Inc - September 24, 2015

Record Details

DRF Medical Group Inc in Louisville, KY was inspected from September 22-24, 2015. The inspection revealed a significant deficiency in the firm's quality system, specifically the absence of established and implemented procedures for corrective and preventive actions (CAPA). This indicates a fundamental weakness in addressing and preventing quality problems related to products and the quality system.

Company
DRF Medical Group Inc
Inspection date
September 24, 2015
Product type
device
Office
Cincinnati District Office
Person
  • Teresa Kastner (Consumer Safety Officer, Medical Device Specialist)
View Company Profile

ID · aaeee740-5754-4b58-b6e2-eb4215adda3c

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