# FDA Inspection 1060869 - Shenzhen OKFAN Electronics Co., Ltd. - December 08, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/shenzhen-okfan-electronics-co-ltd/4b90884b-e629-4776-b9af-9120b7e139ee
Source feed: FDA_Inspections

> FDA Inspection 1060869 for Shenzhen OKFAN Electronics Co., Ltd. on December 08, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1060869
- Company Name: Shenzhen OKFAN Electronics Co., Ltd.
- Inspection Date: 2017-12-08
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/shenzhen-okfan-electronics-co-ltd/420a0e27-fbe2-42dd-bbb9-9e0b643dd812

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