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483
•Proven Process Medical Devices, Inc.•December 13, 2019

Proven Process Medical Devices, Inc. – FDA 483, Dec 13, 2019

Record Details

An FDA inspection of Proven Process Medical Devices, Inc. in Mansfield, MA, a contract manufacturer, revealed significant deficiencies in their quality management system. The firm failed to establish adequate procedures for corrective and preventive actions, control of non-conforming product, and ensure the suitability and maintenance of inspection and test equipment. These observations indicate a need for comprehensive improvements in their manufacturing and quality control processes.

Company
Proven Process Medical Devices, Inc.
Inspection date
December 13, 2019
Product type
device
Office
Division of Northeast Imports 
Person
  • Maryam Tabatabaie (issuing_officer)
View Company Profile

ID · 73890ab3-7d70-4004-8167-ad1d4d61cd80

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