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FDA Inspection
•Suzhou Jingle Polymer Medical Apparatus Co., Ltd.•January 19, 2017

Suzhou Jingle Polymer Medical Apparatus Co., Ltd. – FDA Inspection, Jan 19, 2017

Record Details

This FDA Inspection record concerns Suzhou Jingle Polymer Medical Apparatus Co., Ltd., with an inspection on January 19, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Suzhou Jingle Polymer Medical Apparatus Co., Ltd.
Inspection Date
January 19, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Felix J. Marrero (Issuing Officer)
View Company Profile

ID · 8ac8f853-b0bc-4925-b325-8443930ae5b3

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1013104
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

Other FDA inspections of Suzhou Jingle Polymer Medical Apparatus Co., Ltd.

1
DateClassificationOfficeProject area
May 22, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Suzhou Jingle Polymer Medical Apparatus Co., Ltd.
  • FDA Inspection 881041 - 2014-05-22

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