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Sentry Manufacturing, Inc.

FDA Regulatory Profile

Sentry Manufacturing, Inc. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 21, 2026 · 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
Jul 21, 2026Miami Lakes, FLFood/CosmeticsNo Action Indicated (NAI)1051353
Jun 2, 2023Miami Lakes, FLFood/CosmeticsNo Action Indicated (NAI)1051353
Sep 27, 2019Miami Lakes, FLFood/CosmeticsNo Action Indicated (NAI)1051353
Sep 14, 2016Miami Lakes, FLFood/CosmeticsNo Action Indicated (NAI)1051353
Jul 18, 2012Miami Lakes, FLFood/CosmeticsNo Action Indicated (NAI)1051353

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 1051353Miami Lakes, FL5Jul 21, 2026

FDA data resources

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