Dester Corporation

FDA Regulatory Profile

Dester Corporation has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Dester Corporation" and its spelling variant "Dester Company Limited".

Latest inspection
Jun 23, 2026 · VAI

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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
Inspections5Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA Record by Year

Dester Corporation's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Dester Corporation: FDA inspections per year 2017: 0 inspections020172018: 0 inspections020182019: 0 inspections020192020: 0 inspections020202021: 0 inspections020212022: 1 inspections120222023: 2 inspections220232024: 1 inspections120242025: 0 inspections020252026: 1 inspections12026
YearInspectionsOAIWarning lettersRecall recordsClass I
202610000
202500000
202410000
202320000
202210000
202100000
202000000
201900000
201800000
201700000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA Inspections

5 inspections from Mar 31, 2022 to Jun 23, 2026.

DateSiteProductClassificationFEI
Jun 23, 2026Atlanta, GAFood/CosmeticsVoluntary Action Indicated (VAI)3027681977
Dec 4, 2024Si Maha Phot, ThailandFood/CosmeticsNo Action Indicated (NAI)3006634455
Apr 20, 2023Lima, OHFood/CosmeticsVoluntary Action Indicated (VAI)3014517174
Mar 23, 2023College Park, GAFood/CosmeticsVoluntary Action Indicated (VAI)3009731017
Mar 31, 2022College Park, GAFood/CosmeticsVoluntary Action Indicated (VAI)3009731017

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

4 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3027681977Atlanta, GA1Jun 23, 2026
FEI 3006634455Si Maha Phot, Thailand1Dec 4, 2024
FEI 3014517174Lima, OH1Apr 20, 2023
FEI 3009731017College Park, GA2Mar 23, 2023

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