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Myriad Fiber Imaging Technologies, Inc.

FDA Regulatory Profile

Myriad Fiber Imaging Technologies, Inc. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 31, 2025 · NAI

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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 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 31, 2025Dudley, MADevicesNo Action Indicated (NAI)3002516162
Jul 29, 2022Dudley, MADevicesVoluntary Action Indicated (VAI)3002516162
Sep 18, 2015Dudley, MADevicesVoluntary Action Indicated (VAI)3002516162
Feb 7, 2012Dudley, MADevicesNo Action Indicated (NAI)3002516162

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 3002516162Dudley, MA4Jul 31, 2025

FDA data resources

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