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Right Dose, Inc.

FDA Regulatory Profile

Right Dose, Inc. has 0 FDA recalls, 3 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Aug 29, 2019 · NAI
Latest 510(k)
Aug 18, 2017

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances1Oct 4, 2026Not statedCurrent
Inspections3Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 29, 2019Port Washington, NYDevicesNo Action Indicated (NAI)3009761898
Jul 16, 2015Port Washington, NYDevicesNo Action Indicated (NAI)3009761898
Mar 14, 2013Port Washington, NYDevicesNo Action Indicated (NAI)3009761898

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.

Recent 510(k) Clearances

K-NumberDeviceDate
K171261ScannerSide DoseCheckAug 18, 2017

FDA data resources