VitaNorth USA, LLC FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

VitaNorth USA, LLC has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "VitaNorth USA, LLC" is on file.

What these totals cover: FDA records filed under the name "VitaNorth USA, LLC" and its spelling variant "Vitanorth Usa".

Latest inspection
Aug 24, 2026 · VAI

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 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

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

VitaNorth USA, LLC: FDA inspections per year 2017: 0 inspections020172018: 0 inspections020182019: 0 inspections020192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 1 inspections120232024: 0 inspections020242025: 2 inspections220252026: 1 inspections12026
YearInspectionsOAIWarning lettersRecall recordsClass I
202610000
202520000
202400000
202310000
202200000
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.

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Recent FDA inspections

4 inspections from Feb 22, 2023 to Aug 24, 2026.

DateSiteProductClassificationFEI
Aug 24, 2026Westland, MIFood/CosmeticsVoluntary Action Indicated (VAI)3037591809
Apr 17, 2025Westland, MIFood/CosmeticsVoluntary Action Indicated (VAI)3013030652
Apr 17, 2025Westland, MIFood/CosmeticsVoluntary Action Indicated (VAI)3037591809
Feb 22, 2023Westland, MIFood/CosmeticsVoluntary Action Indicated (VAI)3013030652
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
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

2 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3037591809Westland, MI2Aug 24, 2026
FEI 3013030652Westland, MI2Apr 17, 2025

VitaNorth USA, LLC and the FDA: common questions

Has VitaNorth USA, LLC received an FDA warning letter?

No FDA warning letter addressed to the name "VitaNorth USA, LLC" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has VitaNorth USA, LLC received an FDA Form 483?

FDA has not published a Form 483 for "VitaNorth USA, LLC" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect VitaNorth USA, LLC?

The most recent FDA inspection on file ended Aug 24, 2026 at Westland, MI and was classified VAI. FDA has 4 inspections of VitaNorth USA, LLC on file.

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