# FDA Inspection 881041 - Suzhou Jingle Polymer Medical Apparatus Co., Ltd. - May 22, 2014

Source: https://www.keypedia.com/records/fda_inspections/suzhou-jingle-polymer-medical-apparatus-co-ltd/794ef17a-7dfd-47dd-b0b1-e57cfce29bd1
Source feed: FDA_Inspections

> FDA Inspection 881041 for Suzhou Jingle Polymer Medical Apparatus Co., Ltd. on May 22, 2014. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 881041
- Company Name: Suzhou Jingle Polymer Medical Apparatus Co., Ltd.
- Inspection Date: 2014-05-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1013104 - 2017-01-19](https://www.keypedia.com/records/fda_inspections/suzhou-jingle-polymer-medical-apparatus-co-ltd/8ac8f853-b0bc-4925-b325-8443930ae5b3)
- [FDA Inspection 881041 - 2014-05-22](https://www.keypedia.com/records/fda_inspections/suzhou-jingle-polymer-medical-apparatus-co-ltd/cf14c950-ae4a-4b62-921d-898a0ce14d8e)

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