# Shenzhen Kaiyan Medical Equipment Limited – FDA Inspection, Oct 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-kaiyan-medical-equipment-limited/379b7668-d23f-460d-bc53-d7930da0dece
Source feed: FDA_Inspections

> FDA inspection 1032564 of Shenzhen Kaiyan Medical Equipment Limited, October 25, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1032564
- Company Name: Shenzhen Kaiyan Medical Equipment Limited
- Inspection Date: 2017-10-25
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/miaja-umaedi/0a41661f-08bb-4523-ab09-b17e230068e0)

Company: https://www.keypedia.com/companies/shenzhen-kaiyan-medical-equipment-limited/b7a22378-ecf5-410a-9359-bbebf4ad9283

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