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Menasha Packaging Company LLC

FDA Regulatory Profile

Menasha Packaging Company LLC has 0 FDA recalls, 30 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 23, 2026 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections30Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 23, 2026Lebanon, PADrugsVoluntary Action Indicated (VAI)3021035729
Nov 20, 2025Lewisville, TXFood/CosmeticsNo Action Indicated (NAI)3017199965
Nov 14, 2025Edwardsville, ILDrugsNo Action Indicated (NAI)3010749695
Nov 6, 2025Lititz, PADrugsVoluntary Action Indicated (VAI)3030004310
Feb 18, 2025Edison, NJDevicesNo Action Indicated (NAI)3010687142
Aug 23, 2023Winchester, VAFood/CosmeticsNo Action Indicated (NAI)3016750403
Aug 16, 2023Lebanon, PADrugsNo Action Indicated (NAI)3021035729
May 23, 2023Edison, NJFood/CosmeticsNo Action Indicated (NAI)3010687142
Jan 23, 2023Fontana, CADrugsNo Action Indicated (NAI)3022221320
Aug 10, 2022Edison, NJDrugsNo Action Indicated (NAI)3010687142
Feb 20, 2020Newville, PADevicesNo Action Indicated (NAI)3004764532
Dec 4, 2019Edison, NJDevicesNo Action Indicated (NAI)3010687142
Aug 21, 2019Edwardsville, ILDrugsNo Action Indicated (NAI)3010749695
May 23, 2018Lithia Springs, GADrugsNo Action Indicated (NAI)3014160467
Jun 9, 2017Tobyhanna, PADrugsNo Action Indicated (NAI)3007135543
Apr 5, 2017Rock Island, ILDrugsNo Action Indicated (NAI)3004046580
Nov 30, 2016Edison, NJDrugsVoluntary Action Indicated (VAI)3010687142
Sep 1, 2016Winchester, VAFood/CosmeticsNo Action Indicated (NAI)3016750403
Oct 2, 2014Edison, NJDrugsNo Action Indicated (NAI)3010687142
Feb 12, 2013Edwardsville, ILDrugsNo Action Indicated (NAI)3007334763

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.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3021035729Lebanon, PA2Jun 23, 2026
FEI 3017199965Lewisville, TX1Nov 20, 2025
FEI 3010749695Edwardsville, IL4Nov 14, 2025
FEI 3030004310Lititz, PA1Nov 6, 2025
FEI 3010687142Edison, NJ8Feb 18, 2025
FEI 3016750403Winchester, VA2Aug 23, 2023
FEI 3022221320Fontana, CA1Jan 23, 2023
FEI 3004764532Newville, PA2Feb 20, 2020
FEI 3014160467Lithia Springs, GA1May 23, 2018
FEI 3007135543Tobyhanna, PA2Jun 9, 2017
FEI 3004046580Rock Island, IL2Apr 5, 2017
FEI 3007334763Edwardsville, IL1Feb 12, 2013
FEI 3004046684Hodgkins, IL2Feb 15, 2011
FEI 3007056962Aurora, IL1Mar 2, 2010

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.