# FDA Inspection 1101816 - Ningbo Luke Medical Devices Co., Ltd. - September 05, 2019

Source: https://www.keypedia.com/records/fda_inspections/ningbo-luke-medical-devices-co-ltd/70b67696-6ee3-47a6-9939-5f48a20f381e
Source feed: FDA_Inspections

> FDA Inspection 1101816 for Ningbo Luke Medical Devices Co., Ltd. on September 05, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101816
- Company Name: Ningbo Luke Medical Devices Co., Ltd.
- Inspection Date: 2019-09-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1101816 - 2019-09-05](https://www.keypedia.com/records/fda_inspections/ningbo-luke-medical-devices-co-ltd/5f51ca23-42fe-4628-9cc3-35049b49e8d4)

Company: https://www.keypedia.com/companies/ningbo-luke-medical-devices-co-ltd/b59cc89a-2e76-444b-8acf-212a95ab6b9a

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