Salazones Garre, S.L. FDA Record

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

Salazones Garre, S.L. has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 2 compliance actions on record. FDA has issued 2 warning letters to Salazones Garre, S.L., the most recent on Jan 28, 2019.

What these totals cover: FDA records filed under the name "Salazones Garre, S.L." and its spelling variant "Salazones Garre, S.L".

Latest inspection
Jul 9, 2018 · OAI

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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
Inspections2Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

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

Salazones Garre, S.L.: FDA inspections per year 2017: 0 inspections020172018: 1 inspections120182019: 0 inspections020192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 0 inspections020232024: 0 inspections020242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400000
202300000
202200000
202100000
202000000
201900100
201811000
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.

Salazones Garre, S.L. FDA Warning Letters

2 warning letters from Nov 6, 2014 to Jan 28, 2019.

IssuedSubjectIssuing officeClose-out letter
Jan 28, 2019
Nov 6, 2014

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

2 inspections from May 6, 2014 to Jul 9, 2018.

DateSiteProductClassificationFEI
Jul 9, 2018San Pedro Del Pinatar, SpainFood/CosmeticsOfficial Action Indicated (OAI)3006285532
May 6, 2014San Pedro Del Pinatar, SpainFood/CosmeticsOfficial Action Indicated (OAI)3006285532
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.

Compliance Actions

FDA's compliance actions data lists 2 compliance actions under Salazones Garre, S.L.: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Jan 28, 2019.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3006285532San Pedro Del Pinatar, Spain2Jul 9, 2018

Salazones Garre, S.L. and the FDA: common questions

Has Salazones Garre, S.L. received an FDA warning letter?

Yes. FDA has issued 2 warning letters to Salazones Garre, S.L.. The most recent is dated Jan 28, 2019.

Has Salazones Garre, S.L. received an FDA Form 483?

FDA has not published a Form 483 for "Salazones Garre, S.L." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Salazones Garre, S.L.?

The most recent FDA inspection on file ended Jul 9, 2018 at San Pedro Del Pinatar, Spain and was classified OAI. FDA has 2 inspections of Salazones Garre, S.L. on file, 2 of them classified OAI (official action indicated).

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