Johnson Brothers Liquor Company, Inc FDA Record

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

Johnson Brothers Liquor Company, Inc has 2 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Johnson Brothers Liquor Company, Inc" is on file.

What these totals cover: FDA records filed under the name "Johnson Brothers Liquor Company, Inc" and its spelling variants "Johnson Brothers Liquor Company", "Johnson Brothers Liquor".

Latest recall
F-1815-2013 · Class II · Jul 24, 2013
Latest inspection
Mar 11, 2026 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls2Nov 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

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

Johnson Brothers Liquor Company, Inc: FDA inspections per year 2017: 1 inspections120172018: 0 inspections020182019: 0 inspections020192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 0 inspections020232024: 0 inspections020242025: 1 inspections120252026: 1 inspections12026
YearInspectionsOAIWarning lettersRecall recordsClass I
202610000
202510000
202400000
202300000
202200000
202100000
202000000
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 recalls

2 recall records on Jul 24, 2013.

NumberClassProductDate
F-1815-2013Class IIEvviva Strawberry Spumante, UPC 84279-99138Jul 24, 2013
F-1814-2013Class IIEvviva Fresh Peach Spumante, UPC 84279-99137Jul 24, 2013

Recent FDA inspections

4 inspections from Dec 19, 2012 to Mar 11, 2026.

DateSiteProductClassificationFEI
Mar 11, 2026Saint Paul, MNFood/CosmeticsVoluntary Action Indicated (VAI)1000347228
Nov 4, 2025Mendota Heights, MNFood/CosmeticsNo Action Indicated (NAI)3013721545
Sep 25, 2017Saint Paul, MNFood/CosmeticsNo Action Indicated (NAI)1000347228
Dec 19, 2012Saint Paul, MNFood/CosmeticsNo Action Indicated (NAI)1000347228
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 1000347228Saint Paul, MN3Mar 11, 2026
FEI 3013721545Mendota Heights, MN1Nov 4, 2025

Johnson Brothers Liquor Company, Inc and the FDA: common questions

Has Johnson Brothers Liquor Company, Inc received an FDA warning letter?

No FDA warning letter addressed to the name "Johnson Brothers Liquor Company, Inc" 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 Johnson Brothers Liquor Company, Inc received an FDA Form 483?

FDA has not published a Form 483 for "Johnson Brothers Liquor Company, Inc" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Johnson Brothers Liquor Company, Inc?

The most recent FDA inspection on file ended Mar 11, 2026 at Saint Paul, MN and was classified VAI. FDA has 4 inspections of Johnson Brothers Liquor Company, Inc on file.

Has Johnson Brothers Liquor Company, Inc had an FDA recall?

Yes. Johnson Brothers Liquor Company, Inc has 2 FDA recalls on record. The most recent started Jul 24, 2013.

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