Maria Candela Etchegaray FDA Record

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

Maria Candela Etchegaray has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Maria Candela Etchegaray" is on file.

What these totals cover: FDA records filed under the name "Maria Candela Etchegaray".

Latest inspection
Mar 31, 2025 · NAI

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 actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent FDA inspections

1 inspection on Mar 31, 2025.

DateSiteProductClassificationFEI
Mar 31, 2025Buenos Aires, ArgentinaDrugsNo Action Indicated (NAI)3033814158
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 3033814158Buenos Aires, Argentina1Mar 31, 2025

Maria Candela Etchegaray and the FDA: common questions

Has Maria Candela Etchegaray received an FDA warning letter?

No FDA warning letter addressed to the name "Maria Candela Etchegaray" 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 Maria Candela Etchegaray received an FDA Form 483?

FDA has not published a Form 483 for "Maria Candela Etchegaray" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Maria Candela Etchegaray?

The most recent FDA inspection on file ended Mar 31, 2025 at Buenos Aires, Argentina and was classified NAI. FDA has 1 inspection of Maria Candela Etchegaray on file.

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