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Almota Elevator Company Inc

FDA Regulatory Profile

Almota Elevator Company Inc has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Almota Elevator Company Inc" and its spelling variant "Almota Elevator Company".

Latest inspection
Sep 8, 2017 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections4Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

4 inspections from Sep 20, 2012 to Sep 8, 2017.

DateSiteProductClassificationFEI
Sep 8, 2017Colfax, WAFood/CosmeticsNo Action Indicated (NAI)3014999
Mar 31, 2014Colfax, WAFood/CosmeticsNo Action Indicated (NAI)3015749
Mar 31, 2014Colfax, WAFood/CosmeticsNo Action Indicated (NAI)3015954
Sep 20, 2012Colfax, WAFood/CosmeticsNo Action Indicated (NAI)3014999

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.

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FDA-Inspected Facilities

3 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3014999Colfax, WA2Sep 8, 2017
FEI 3015749Colfax, WA1Mar 31, 2014
FEI 3015954Colfax, WA1Mar 31, 2014

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FDA data resources

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