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Santa Barbara Imaging Systems

FDA Regulatory Profile

Santa Barbara Imaging Systems has 0 FDA recalls, 1 inspection, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Apr 16, 2018 · NAI
Latest 510(k)
Feb 28, 2023

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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
Inspections1Oct 27, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 16, 2018Goleta, CADevicesNo Action Indicated (NAI)3011373951

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
K2231168X-10-6XXX Camera HeadFeb 28, 2023
K1525138X-10-XXXX Camera SystemDec 15, 2015

FDA data resources