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LPNA Group Inc.

FDA Regulatory Profile

LPNA Group Inc. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jan 21, 2026 · VAI

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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
Inspections8Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 21, 2026Tonawanda, NYDrugsVoluntary Action Indicated (VAI)1000120219
Jun 5, 2025Tonawanda, NYFood/CosmeticsNo Action Indicated (NAI)1000120219
Apr 11, 2023Tonawanda, NYDrugsVoluntary Action Indicated (VAI)1000120219
Dec 18, 2015Tonawanda, NYDrugsNo Action Indicated (NAI)1000120219
Jun 7, 2013Tonawanda, NYDrugsNo Action Indicated (NAI)1000120219
Mar 7, 2011Tonawanda, NYDrugsNo Action Indicated (NAI)1000120219
May 7, 2010Tonawanda, NYDrugsVoluntary Action Indicated (VAI)1000120219
Oct 20, 2008Tonawanda, NYDrugsNo Action Indicated (NAI)1000120219

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 1000120219Tonawanda, NY8Jan 21, 2026

FDA data resources

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