Shanghai Kindly Enterprise Development Group Co., Ltd.

FDA Regulatory Profile

Shanghai Kindly Enterprise Development Group Co., Ltd. has 0 FDA recalls, 3 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 9, 2018 · NAI
Latest 510(k)
Feb 16, 2023

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances2Oct 4, 2026Not statedCurrent
Inspections3Oct 27, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 9, 2018Jiading, ChinaDevicesNo Action Indicated (NAI)3005405146
Oct 10, 2013Jiading, ChinaDevicesVoluntary Action Indicated (VAI)3005405146
Jul 19, 2011Jiading, ChinaDevicesVoluntary Action Indicated (VAI)3005405146

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K223327Sterile Aesthetic Cannula and Hypodermic NeedleFeb 16, 2023
K223678Sterile Syringes for Single UseFeb 9, 2023