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Media Plus, LLC

FDA Regulatory Profile

Media Plus, LLC has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Jan 27, 2025 · NAI
Latest 510(k)
Jun 1, 2018

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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
Inspections2Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 27, 2025Englewood Cliffs, NJDevicesNo Action Indicated (NAI)3015176320
Mar 10, 2023Englewood Cliffs, NJDevicesVoluntary Action Indicated (VAI)3015176320

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
K171798Silverwear Silver Pro Garment DeviceJun 1, 2018

FDA data resources