Glicerinas Industriales, S.A De C.V FDA Record

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

  • Latest inspection OAI · May 12, 2023
  • Last warning letter 2024
Inspections 1 1 OAI
Recalls 0 0 Class I
Warning letters 2 Latest Jan 16, 2024
510(k) clearances 0 None on file

Glicerinas Industriales, S.A De C.V has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 2 compliance actions on record. FDA has issued 2 warning letters to Glicerinas Industriales, S.A De C.V, the most recent on Jan 16, 2024.

What these totals cover: FDA records filed under the name "Glicerinas Industriales, S.A De C.V".

Latest inspection
May 12, 2023 · OAI

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
Inspections1Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Glicerinas Industriales, S.A De C.V's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Glicerinas Industriales, S.A De C.V: FDA inspections per year

YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400100
202311000
202200100
202100000
202000000
201900000
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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Glicerinas Industriales, S.A De C.V FDA Warning Letters

2 warning letters from Jun 14, 2022 to Jan 16, 2024.

IssuedSubjectIssuing officeClose-out letter
Jan 16, 2024 · Record page
Jun 14, 2022 · Record page

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

1 inspection on May 12, 2023.

DateSiteProductClassificationFEI
May 12, 2023Zapopan, MexicoDrugsOfficial Action Indicated (OAI)3016420687
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 Glicerinas Industriales, S.A De C.V: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Jan 16, 2024.

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 3016420687Zapopan, Mexico1May 12, 2023

Glicerinas Industriales, S.A De C.V and the FDA: common questions

Has Glicerinas Industriales, S.A De C.V received an FDA warning letter?

Yes. FDA has issued 2 warning letters to Glicerinas Industriales, S.A De C.V. The most recent is dated Jan 16, 2024.

Has Glicerinas Industriales, S.A De C.V received an FDA Form 483?

FDA has not published a Form 483 for "Glicerinas Industriales, S.A De C.V" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Glicerinas Industriales, S.A De C.V?

The most recent FDA inspection on file ended May 12, 2023 at Zapopan, Mexico and was classified OAI. FDA has 1 inspection of Glicerinas Industriales, S.A De C.V 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.