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Ningbo Hesi Electric Co., Ltd.

FDA Regulatory Profile

Ningbo Hesi Electric Co., Ltd. has 0 FDA recalls, 1 inspection, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Feb 10, 2023 · VAI
Latest 510(k)
Jul 14, 2021

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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) clearances1Oct 4, 2026Not statedCurrent
Inspections1Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 10, 2023Ningbo, ChinaDevicesVoluntary Action Indicated (VAI)3009784099

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
K200983Infrared light therapy led facial light therapy mask-Derma plus, Photons Facial Skin Care Machine…Jul 14, 2021

FDA data resources