FDA Inspection
Turnxon Precision Co.,Ltd.Turnxon Precision Co.,Ltd. – FDA Inspection, Jul 12, 2017
Record Details
This FDA Inspection record concerns Turnxon Precision Co.,Ltd., with an inspection on July 12, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · e07ca575-2c33-4427-ad60-5a60fee0ff16
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1019289
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.22Quality audits - Lack of or inadequate procedures
- 21 CFR 820.30(h)Design transfer - Lack of or inadequate procedures
- 21 CFR 820.75(a)Documentation
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Other FDA inspections of Turnxon Precision Co.,Ltd.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| December 11, 2025 | NAI | Postmarket Assurance: Devices |
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