Micro Tool Engineering, Inc.

FDA Regulatory Profile

Micro Tool Engineering, Inc. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 12, 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
Inspections5Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 12, 2025Riviera Beach, FLDevicesNo Action Indicated (NAI)3003925093
May 22, 2023Riviera Beach, FLDevicesNo Action Indicated (NAI)3003925093
Jun 14, 2019Riviera Beach, FLDevicesNo Action Indicated (NAI)3003925093
Aug 8, 2013Riviera Beach, FLDevicesNo Action Indicated (NAI)3003925093
Dec 4, 2009Riviera Beach, FLDevicesVoluntary Action Indicated (VAI)3003925093

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 3003925093Riviera Beach, FL5Sep 12, 2025

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