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FDA Inspection
•Jiangxi Sanxin MedTec Co., Ltd.•July 31, 2014

Jiangxi Sanxin MedTec Co., Ltd. – FDA Inspection, Jul 31, 2014

Record Details

This FDA Inspection record concerns Jiangxi Sanxin MedTec Co., Ltd., with an inspection on July 31, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company
Jiangxi Sanxin MedTec Co., Ltd.
Inspection Date
July 31, 2014
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 6644aa12-e201-4866-989b-5f6ca5dab885

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
890434
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

3
  1. 21 CFR 820.72(b)Calibration procedures - content
  2. 21 CFR 820.70(e)Contamination control, Lack of or inadequate procedures
  3. 21 CFR 820.70(d)Implementing Personnel Procedures, Health, Cleanliness.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Jiangxi Sanxin MedTec Co., Ltd.

1
DateClassificationOfficeProject area
June 25, 2025Not classifiedOffice of Inspections and Investigations
Other documents for Jiangxi Sanxin MedTec Co., Ltd.
  • FDA Inspection 1276531 - 2025-06-25

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