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One Way Drug

FDA Regulatory Profile

One Way Drug has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 2 compliance actions on record.

Latest inspection
Nov 25, 2019 · 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
Inspections4Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 25, 2019Las Vegas, NVDrugsVoluntary Action Indicated (VAI)3011769075
Mar 8, 2018Las Vegas, NVDrugsOfficial Action Indicated (OAI)3011769075
Jul 19, 2017Las Vegas, NVDrugsOfficial Action Indicated (OAI)3010839113
May 30, 2014Las Vegas, NVDrugsOfficial Action Indicated (OAI)3010839113

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 3011769075Las Vegas, NV2Nov 25, 2019
FEI 3010839113Las Vegas, NV2Jul 19, 2017

FDA data resources

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