Gray & Company

FDA Regulatory Profile

Gray & Company has 0 FDA recalls, 9 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 26, 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
Inspections9Nov 12, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 26, 2017Traverse City, MIFood/CosmeticsNo Action Indicated (NAI)1812847
Mar 28, 2017Dayton, ORFood/CosmeticsVoluntary Action Indicated (VAI)3014871
Jan 10, 2017Hart, MIFood/CosmeticsNo Action Indicated (NAI)3004692372
May 11, 2016Dayton, ORFood/CosmeticsVoluntary Action Indicated (VAI)3014871
Dec 17, 2014Hart, MIFood/CosmeticsNo Action Indicated (NAI)1824751
Apr 30, 2012Hart, MIFood/CosmeticsNo Action Indicated (NAI)1824751
Oct 25, 2011Forest Grove, ORFood/CosmeticsVoluntary Action Indicated (VAI)3010827
Jul 28, 2011Dayton, ORFood/CosmeticsVoluntary Action Indicated (VAI)3014871
Oct 24, 2008Traverse City, MIFood/CosmeticsNo Action Indicated (NAI)1812847

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.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 1812847Traverse City, MI2Jul 26, 2017
FEI 3014871Dayton, OR3Mar 28, 2017
FEI 3004692372Hart, MI1Jan 10, 2017
FEI 1824751Hart, MI2Dec 17, 2014
FEI 3010827Forest Grove, OR1Oct 25, 2011

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