Marich Confectionery Company, Inc. FDA Record

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

Marich Confectionery Company, Inc. has 2 FDA recalls (1 Class I), 3 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Marich Confectionery Company, Inc." is on file.

What these totals cover: FDA records filed under the name "Marich Confectionery Company, Inc." and its spelling variant "Marich Confectionery Company".

Latest recall
F-0726-2019 · Class I · Nov 16, 2018
Latest inspection
Apr 25, 2025 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls2 (1 Class I)Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections3Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

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

Marich Confectionery Company, Inc.: FDA inspections per year 2017: 0 inspections020172018: 0 inspections020182019: 0 inspections020192020: 0 inspections020202021: 1 inspections120212022: 0 inspections020222023: 0 inspections020232024: 0 inspections020242025: 2 inspections220252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202520000
202400000
202300000
202200000
202110000
202000000
201900000
201800011
201700010

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 from Jan 25, 2017 to Nov 16, 2018.

NumberClassProductDate
F-0726-2019Class IMilk Chocolate Maltballs: NET Wt. 15 lbs. Item number 992 Case UPC 00797817-00992-9 Allergy…Nov 16, 2018
F-1451-2017Class IIMARICH Premium Chocolates; Chocolate Caramel Heart; Our delicious caramel hearts in rich milk and…Jan 25, 2017

Recent FDA inspections

3 inspections from Aug 26, 2021 to Apr 25, 2025.

DateSiteProductClassificationFEI
Apr 25, 2025Hollister, CAFood/CosmeticsVoluntary Action Indicated (VAI)3003019581
Apr 25, 2025Hollister, CAFood/CosmeticsNo Action Indicated (NAI)3003019581
Aug 26, 2021Hollister, CAFood/CosmeticsVoluntary Action Indicated (VAI)3003019581
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

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3003019581Hollister, CA3Apr 25, 2025

Marich Confectionery Company, Inc. and the FDA: common questions

Has Marich Confectionery Company, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "Marich Confectionery 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 Marich Confectionery Company, Inc. received an FDA Form 483?

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

When did the FDA last inspect Marich Confectionery Company, Inc.?

The most recent FDA inspection on file ended Apr 25, 2025 at Hollister, CA and was classified VAI. FDA has 3 inspections of Marich Confectionery Company, Inc. on file.

Has Marich Confectionery Company, Inc. had an FDA recall?

Yes. Marich Confectionery Company, Inc. has 2 FDA recalls on record, 1 of them Class I, the most serious class. The most recent started Nov 16, 2018.

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