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Interfries Inc.

FDA Regulatory Profile

Interfries 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 "Interfries Inc." and its spelling variant "Interfries".

Latest inspection
Sep 13, 2023 · 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

FDA Record by Year

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

Interfries Inc.: FDA inspections per year 2017: 1 inspections120172018: 0 inspections020182019: 0 inspections020192020: 1 inspections120202021: 0 inspections020212022: 1 inspections120222023: 1 inspections120232024: 0 inspections020242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400000
202310000
202210000
202100000
202010000
201900000
201800000
201710000

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

4 inspections from Sep 26, 2017 to Sep 13, 2023.

DateSiteProductClassificationFEI
Sep 13, 2023Miami, FLFood/CosmeticsNo Action Indicated (NAI)3013055434
Jul 12, 2022Miami, FLFood/CosmeticsVoluntary Action Indicated (VAI)3013055434
Jul 13, 2020Miami, FLFood/CosmeticsVoluntary Action Indicated (VAI)3013055434
Sep 26, 2017Miami, FLFood/CosmeticsNo Action Indicated (NAI)3013055434

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

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3013055434Miami, FL4Sep 13, 2023

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FDA data resources

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