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483
•Illuminoss Medical Inc.•September 24, 2019

Illuminoss Medical Inc. – FDA 483, Sep 24, 2019

Record Details

Illuminoss Medical, a medical device manufacturer in East Providence, RI, was cited for multiple quality system deficiencies during an FDA inspection. The observations primarily concern failures in Medical Device Reporting (MDR), control of nonconforming product, supplier qualification, equipment suitability, and complaint handling procedures. These issues indicate a lack of adequate controls to ensure product quality and compliance with regulatory requirements.

Company
Illuminoss Medical Inc.
Inspection date
September 24, 2019
Product type
device
Office
Division of Northeast Imports 
Person
  • Maryam Tabatabaie (issuing_officer)
View Company Profile

ID · d6f9e380-6ecd-42eb-ae00-c0c32bfff308

Other documents for Illuminoss Medical Inc.
  • 483 - 2024-02-01February 1, 2024
  • 483 - 2022-11-02November 2, 2022
  • EIR - 2019-09-24September 24, 2019

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