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FDA Inspection
•Flextronics Electronics Technology (Suzhou) Co., Ltd.•November 8, 2018

Flextronics Electronics Technology (Suzhou) Co., Ltd. – FDA Inspection, Nov 8, 2018

Record Details

This FDA Inspection record concerns Flextronics Electronics Technology (Suzhou) Co., Ltd., with an inspection on November 8, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Flextronics Electronics Technology (Suzhou) Co., Ltd.
Inspection Date
November 8, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Dianiris C. Ayala
View Company Profile

ID · a6676750-7a1d-4f8b-a071-edbdf3ef9bd4

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1071980
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

Other FDA inspections of Flextronics Electronics Technology (Suzhou) Co., Ltd.

2
DateClassificationOfficeProject area
April 21, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
October 16, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Flextronics Electronics Technology (Suzhou) Co., Ltd.
  • FDA Inspection 987247 - 2016-04-21
  • FDA Inspection 903967 - 2014-10-16

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