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K&L Distributing, Inc.

FDA Regulatory Profile

K&L Distributing, Inc. has 0 FDA recalls, 3 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Dec 12, 2019 · NAI
Latest 510(k)
Jan 20, 2023

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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
Inspections3Oct 27, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 12, 2019Decatur, ILFood/CosmeticsNo Action Indicated (NAI)1480011
Apr 4, 2012West Palm Beach, FLFood/CosmeticsNo Action Indicated (NAI)3004665229
Dec 2, 2011Decatur, ILFood/CosmeticsNo Action Indicated (NAI)1480011

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
K222158Capiflo 5001Jan 20, 2023

FDA data resources