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Alltrista Plastics, LLC

FDA Regulatory Profile

Alltrista Plastics, LLC has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 5, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections3Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 5, 2025Greer, SCDevicesNo Action Indicated (NAI)3001237800
Apr 28, 2022Greer, SCDevicesNo Action Indicated (NAI)3001237800
Mar 4, 2020Reedsville, PADevicesVoluntary Action Indicated (VAI)3001236673

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 3001237800Greer, SC2Jun 5, 2025
FEI 3001236673Reedsville, PA1Mar 4, 2020

FDA data resources

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