Universal Packaging Systems, Inc.

FDA Regulatory Profile

Universal Packaging Systems, Inc. has 0 FDA recalls, 15 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 29, 2025 · VAI

Reviewing Universal Packaging Systems, Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Universal Packaging Systems, Inc. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

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
Inspections15Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 29, 2025Chino, CADrugsVoluntary Action Indicated (VAI)1000125370
May 23, 2025Batavia, OHDrugsNo Action Indicated (NAI)3005073265
Nov 17, 2023Chino, CADrugsOfficial Action Indicated (OAI)1000125370
Mar 17, 2023Chino, CADrugsVoluntary Action Indicated (VAI)1000125370
Mar 5, 2019Batavia, OHDevicesVoluntary Action Indicated (VAI)3005073265
Jul 25, 2018Chino, CADrugsNo Action Indicated (NAI)1000125370
Nov 30, 2017Batavia, OHDrugsVoluntary Action Indicated (VAI)3005073265
Dec 22, 2015Chino, CADrugsVoluntary Action Indicated (VAI)1000125370
Dec 19, 2013Batavia, OHDrugsNo Action Indicated (NAI)3005073265
Jun 5, 2013Batavia, OHDrugsNo Action Indicated (NAI)3005073265
Oct 21, 2011Batavia, OHDrugsVoluntary Action Indicated (VAI)3005073265
Jul 8, 2011Batavia, OHDrugsNo Action Indicated (NAI)3005073265
May 4, 2010Batavia, OHDrugsVoluntary Action Indicated (VAI)3005073265
Nov 18, 2009Batavia, OHDrugsNo Action Indicated (NAI)3005073265
Jul 21, 2009Chino, CADrugsNo Action Indicated (NAI)1000125370

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 1000125370Chino, CA6May 29, 2025
FEI 3005073265Batavia, OH9May 23, 2025

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