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FDA Inspection
•Canwell Medical Co. Ltd.•February 23, 2017

Canwell Medical Co. Ltd. – FDA Inspection, Feb 23, 2017

Record Details

This FDA Inspection record concerns Canwell Medical Co. Ltd., with an inspection on February 23, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Canwell Medical Co. Ltd.
Inspection Date
February 23, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Joseph R. Strelnik (FDA Associated Person)
View Company Profile

ID · ad511fdf-c52f-499d-8a0e-999790933bb8

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1009911
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

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