# FDA Inspection 905189 - Guangzhou Aokewei Electronic Co., Ltd. - November 13, 2014

Source: https://www.keypedia.com/records/fda_inspections/guangzhou-aokewei-electronic-co-ltd/4c76b98d-eab8-4a8a-9daf-db448c8e02d5
Source feed: FDA_Inspections

> FDA Inspection 905189 for Guangzhou Aokewei Electronic Co., Ltd. on November 13, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 905189
- Company Name: Guangzhou Aokewei Electronic Co., Ltd.
- Inspection Date: 2014-11-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 905189 - 2014-11-13](https://www.keypedia.com/records/fda_inspections/guangzhou-aokewei-electronic-co-ltd/7855bed5-a3bb-43a9-95f6-6d90699a1065)

Company: https://www.keypedia.com/companies/guangzhou-aokewei-electronic-co-ltd/9f107d88-b1ca-4f18-9786-e4595ccc4f36

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