# Xian Airfoil Technology Co., Ltd. – FDA Inspection, Jan 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/xian-airfoil-technology-co-ltd/c56e12f0-b04d-47b7-b70a-0ee021dfccf4
Source feed: FDA_Inspections

> FDA inspection 1000892 of Xian Airfoil Technology Co., Ltd., January 19, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000892
- Company Name: Xian Airfoil Technology Co., Ltd.
- Inspection Date: 2017-01-19
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/thai-t-duong/59737092-2f30-43a7-b23b-36fa7f212c4a)

Company: https://www.keypedia.com/companies/xian-airfoil-technology-co-ltd/eee5653d-715c-4a74-bb99-6483dc43541e

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