Skanray Technologies Pvt, Ltd.

FDA Regulatory Profile

Skanray Technologies Pvt, Ltd. has 0 FDA recalls, 3 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 13, 2012 · NAI
Latest 510(k)
May 25, 2018

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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) clearances2Oct 4, 2026Not statedCurrent
Inspections3Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 13, 2012Mysore, IndiaDevicesNo Action Indicated (NAI)3009001657
Dec 6, 2012Mysore, IndiaDevicesVoluntary Action Indicated (VAI)3002513440
Jun 25, 2010Mysore, IndiaDevicesVoluntary Action Indicated (VAI)3002513440

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
K172147STAR 65May 25, 2018
K150512STAR 90Jun 17, 2015