Attwill Medical Solutions

FDA Regulatory Profile

Attwill Medical Solutions has 0 FDA recalls, 6 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Dec 13, 2021 · VAI
Latest 510(k)
Sep 3, 2020

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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
Inspections6Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 13, 2021Lodi, WIFood/CosmeticsVoluntary Action Indicated (VAI)3004799623
Apr 5, 2018Lodi, WIFood/CosmeticsNo Action Indicated (NAI)3004799623
Nov 4, 2016Lodi, WIFood/CosmeticsVoluntary Action Indicated (VAI)3004799623
Apr 21, 2016Lodi, WIDrugsNo Action Indicated (NAI)3004799623
Sep 27, 2012Lodi, WIFood/CosmeticsVoluntary Action Indicated (VAI)3004799623
Sep 21, 2010Lodi, WIFood/CosmeticsNo Action Indicated (NAI)3004799623

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
K200641HaloGUARD Protective Disc with CHGSep 3, 2020