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TPM Laboratories, Inc.

FDA Regulatory Profile

TPM Laboratories, Inc. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 18, 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
Inspections5Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 18, 2025Cherry Hill, NJDrugsNo Action Indicated (NAI)3003850582
Oct 16, 2018Cherry Hill, NJDrugsNo Action Indicated (NAI)3003850582
Jan 23, 2014Cherry Hill, NJDrugsNo Action Indicated (NAI)3003850582
Dec 7, 2011Cherry Hill, NJDrugsNo Action Indicated (NAI)3003850582
Aug 11, 2009Cherry Hill, NJDrugsNo Action Indicated (NAI)3003850582

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 3003850582Cherry Hill, NJ5Jun 18, 2025

FDA data resources

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