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Ziip, Inc.

FDA Regulatory Profile

Ziip, Inc. has 0 FDA recalls, 1 inspection, 2 510(k) clearances and 1 compliance action on record.

Latest inspection
Jan 12, 2026 · OAI
Latest 510(k)
Sep 23, 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) clearances2Oct 4, 2026Not statedCurrent
Inspections1Oct 25, 2026Not statedCurrent
Compliance actions1Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 12, 2026Pleasant Hill, CADevicesOfficial Action Indicated (OAI)3029740697

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
K212342ZIIP+ DeviceSep 23, 2021
K161484ZIIP DeviceFeb 24, 2017

FDA data resources