# Ningbo Luke Medical Devices Co., Ltd. – FDA Inspection, Sep 5, 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 of Ningbo Luke Medical Devices Co., Ltd., September 05, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

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