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Premiumestore, LLC

FDA Regulatory Profile

Premiumestore, LLC has 0 FDA recalls, 1 inspection, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 17, 2024 · VAI
Latest 510(k)
Jun 15, 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 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 17, 2024Virginia Beach, VADevicesVoluntary Action Indicated (VAI)3016753714

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
K211520Amerishield Surgical MaskJun 15, 2021
K211275AirMax Procedure MaskMay 25, 2021

FDA data resources