Natureplex, LLC

FDA Regulatory Profile

Natureplex, LLC has 0 FDA recalls, 10 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 21, 2026 · NAI
Latest 510(k)
Dec 20, 2018

Updated: recalls Oct 23, 2026 · inspections Oct 23, 2026 · compliance actions Oct 23, 2026.

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Summary

Recalls
0
510(k) Clearances
2
Inspections
10
Compliance Actions
0

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 21, 2026Memphis, TNFood/CosmeticsNo Action Indicated (NAI)3018283409
Jul 24, 2025Olive Branch, MSDrugsOfficial Action Indicated (OAI)3003631744
Dec 18, 2024Olive Branch, MSFood/CosmeticsNo Action Indicated (NAI)3003631744
Jun 6, 2023Memphis, TNFood/CosmeticsNo Action Indicated (NAI)3018283409
Dec 20, 2019Olive Branch, MSDrugsVoluntary Action Indicated (VAI)3003631744
Jul 24, 2015Olive Branch, MSDrugsNo Action Indicated (NAI)3003631744
Feb 14, 2013Olive Branch, MSDrugsNo Action Indicated (NAI)3003631744
Aug 28, 2012Olive Branch, MSDrugsVoluntary Action Indicated (VAI)3003631744
Sep 20, 2010Olive Branch, MSDrugsVoluntary Action Indicated (VAI)3003631744
Feb 6, 2009Olive Branch, MSDrugsOfficial Action Indicated (OAI)3003631744

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
K180828Natureplex Warm Touch Warming JellyDec 20, 2018
K051963BE-CERTAIN PREGNANCY TESTNov 23, 2005