FDA Inspection 928786 — Jiangsu Shenli Medical Production Co., Ltd.

Jiangsu Shenli Medical Production Co., Ltd. — FEI 3003902757

The FDA completed an inspection of Jiangsu Shenli Medical Production Co., Ltd. on May 7, 2015 in Changzhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 7, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Changzhou (China)

Citations

IDCFRDescription
310821 CFR 820.70(e)Contamination control, Lack of or inadequate procedures

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