# Turnxon Precision Co.,Ltd. – FDA Inspection, Jul 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/turnxon-precision-coltd/e07ca575-2c33-4427-ad60-5a60fee0ff16
Source feed: FDA_Inspections

> FDA inspection 1019289 of Turnxon Precision Co.,Ltd., July 12, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1019289
- Company Name: Turnxon Precision Co.,Ltd.
- Inspection Date: 2017-07-12
- 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: 3

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## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

Company: https://www.keypedia.com/companies/turnxon-precision-coltd/6eff540c-5c6e-413b-b52b-ae482bbec549

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