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483
•Flextronics Electronics Technology (Suzhou) Co., Ltd.•November 5, 2018

Flextronics Electronics Technology (Suzhou) Co., Ltd. – FDA 483, Nov 5, 2018

Record Details

During an FDA inspection, Flextronics Electronics Technology (Suzhou) Co., Ltd., a foreign medical device contract manufacturer, received two observations. The firm was cited for inadequately established and implemented procedures for corrective and preventive actions, including insufficient root cause analysis and verification of effectiveness. Additionally, the company failed to adequately control nonconforming products, specifically by not extending investigations to all affected areas and lacking complete documentation for rework activities.

Company
Flextronics Electronics Technology (Suzhou) Co., Ltd.
Inspection date
November 5, 2018
Product type
device
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
Person
  • Dianiris C. Ayala
View Company Profile

ID · 8f9b915d-0447-4776-80aa-e0a9fdf67817

Other documents for Flextronics Electronics Technology (Suzhou) Co., Ltd.
  • 483 - 2018-11-05November 5, 2018
  • 483 - 2018-11-05November 5, 2018
  • WARNING_LETTER - 2014-10-16October 16, 2014

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