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

Source: https://www.keypedia.com/records/fda_inspections/suzhou-jingle-polymer-medical-apparatus-co-ltd/8ac8f853-b0bc-4925-b325-8443930ae5b3
Source feed: FDA_Inspections

> FDA inspection 1013104 of Suzhou Jingle Polymer Medical Apparatus Co., Ltd., January 19, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1013104
- Company Name: Suzhou Jingle Polymer Medical Apparatus Co., Ltd.
- Inspection Date: 2017-01-19
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 881041 - 2014-05-22

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/felix-j-marrero/fe3bf64e-987b-40d9-8a17-754d58e13433)

Company: https://www.keypedia.com/companies/suzhou-jingle-polymer-medical-apparatus-co-ltd/7e689a31-5061-4a03-9fb0-89d10b25f80a

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7