Santa Maura Spice & Garlic Co, Inc. FDA Record

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

  • Latest inspection VAI · Apr 25, 2025
  • 1 Class I recall
  • No warning letters matched by name
Inspections 7 0 OAI
Recalls 1 1 Class I (100%)
Warning letters 0 None on file
510(k) clearances 0 None on file

Santa Maura Spice & Garlic Co, Inc. has 1 FDA recall (1 Class I), 7 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Santa Maura Spice & Garlic Co, Inc." is on file.

What these totals cover: FDA records filed under the name "Santa Maura Spice & Garlic Co, Inc." and its spelling variant "Santa Maura Spice And Garlic Co".

Latest recall
F-0333-2016 · Class I · Oct 22, 2015
Latest inspection
Apr 25, 2025 · VAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls1 (1 Class I)Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections7Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Santa Maura Spice & Garlic Co, Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Santa Maura Spice & Garlic Co, Inc.: FDA inspections per year

YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202510000
202400000
202300000
202200000
202100000
202000000
201910000
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 recalls

1 recall record on Oct 22, 2015.

NumberClassProductDate
F-0333-2016Class IAvocado Leaves (Hoja De Aguacate), Net Wt. 10lbsOct 22, 2015

Recent FDA inspections

7 inspections from Mar 5, 2010 to Apr 25, 2025.

DateSiteProductClassificationFEI
Apr 25, 2025Los Angeles, CAFood/CosmeticsVoluntary Action Indicated (VAI)3000140954
Apr 10, 2019Los Angeles, CAFood/CosmeticsNo Action Indicated (NAI)3000140954
Mar 25, 2016Los Angeles, CAFood/CosmeticsNo Action Indicated (NAI)3000140954
Nov 19, 2015Los Angeles, CAFood/CosmeticsVoluntary Action Indicated (VAI)3000140954
Jul 16, 2015Los Angeles, CAFood/CosmeticsNo Action Indicated (NAI)3000140954
Apr 28, 2011Los Angeles, CAFood/CosmeticsNo Action Indicated (NAI)3000140954
Mar 5, 2010Los Angeles, CAFood/CosmeticsNo Action Indicated (NAI)3000140954
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 3000140954Los Angeles, CA7Apr 25, 2025

Santa Maura Spice & Garlic Co, Inc. and the FDA: common questions

Has Santa Maura Spice & Garlic Co, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "Santa Maura Spice & Garlic Co, 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 Santa Maura Spice & Garlic Co, Inc. received an FDA Form 483?

FDA has not published a Form 483 for "Santa Maura Spice & Garlic Co, Inc." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Santa Maura Spice & Garlic Co, Inc.?

The most recent FDA inspection on file ended Apr 25, 2025 at Los Angeles, CA and was classified VAI. FDA has 7 inspections of Santa Maura Spice & Garlic Co, Inc. on file.

Has Santa Maura Spice & Garlic Co, Inc. had an FDA recall?

Yes. Santa Maura Spice & Garlic Co, Inc. has 1 FDA recall on record, 1 of them Class I, the most serious class. The most recent started Oct 22, 2015.

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