Gialmar - Produtos Alimentares SA FDA Record

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

Gialmar - Produtos Alimentares SA has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Gialmar - Produtos Alimentares SA, the most recent on Oct 2, 2014.

What these totals cover: FDA records filed under the name "Gialmar - Produtos Alimentares SA" and its spelling variants "Gialmar - Produtos Alimentares", "Gialmar-Produtos Alimentares".

Latest inspection
Dec 11, 2019 · 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
Inspections2Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

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Gialmar - Produtos Alimentares SA FDA Warning Letters

1 warning letter on Oct 2, 2014.

IssuedSubjectIssuing officeClose-out letter
Oct 2, 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 Feb 12, 2014 to Dec 11, 2019.

DateSiteProductClassificationFEI
Dec 11, 2019Tondela, PortugalFood/CosmeticsVoluntary Action Indicated (VAI)3011789677
Feb 12, 2014Figueira Da Foz, PortugalFood/CosmeticsOfficial Action Indicated (OAI)3008592400
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 1 compliance action under Gialmar - Produtos Alimentares SA: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Oct 2, 2014.

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

2 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3011789677Tondela, Portugal1Dec 11, 2019
FEI 3008592400Figueira Da Foz, Portugal1Feb 12, 2014

Gialmar - Produtos Alimentares SA and the FDA: common questions

Has Gialmar - Produtos Alimentares SA received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Gialmar - Produtos Alimentares SA. The most recent is dated Oct 2, 2014.

Has Gialmar - Produtos Alimentares SA received an FDA Form 483?

FDA has not published a Form 483 for "Gialmar - Produtos Alimentares SA" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Gialmar - Produtos Alimentares SA?

The most recent FDA inspection on file ended Dec 11, 2019 at Tondela, Portugal and was classified VAI. FDA has 2 inspections of Gialmar - Produtos Alimentares SA on file, 1 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.