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Api-Royal, S.A de CV

FDA import alert and refusal historySan Luis Potosi, MexicoFEI 2000006774

Recorded by FDA as API-ROYAL, S.A DE CV

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Example subjectApi-Royal, S.A de C added to Import Alert 16-129 (red list)

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As of October 26, 2026, Api-Royal, S.A de CV (San Luis Potosi, Mexico) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for linzaa powder (powder drink mix); ultra pina linzaa (powder drink mix); ultra manzana lax powder (powder drink mix), published by FDA on October 2, 2015, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Api-Royal, S.A de CV

1 record, newest first. Each line links to the FDA page it came from.

2015

  1. Import alert listing
    Listed on Import Alert 99-39red listLinzaa powder (powder drink mix); Ultra Pina Linzaa (powder drink mix); Ultra Manzana Lax powder (powder drink mix)
    Source

Questions about Api-Royal, S.A de CV

Is Api-Royal, S.A de CV on an FDA import alert?
Yes. As of October 26, 2026, Api-Royal, S.A de CV is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for linzaa powder (powder drink mix); ultra pina linzaa (powder drink mix); ultra manzana lax powder (powder drink mix); FDA published the listing on October 2, 2015.
Has FDA refused shipments from Api-Royal, S.A de CV?
No FDA import refusals for Api-Royal, S.A de CV appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Api-Royal, S.A de CV's FEI number?
Api-Royal, S.A de CV's FDA Establishment Identifier (FEI) is 2000006774.
Can shipments from Api-Royal, S.A de CV still enter the U.S.?
Shipments of linzaa powder (powder drink mix); ultra pina linzaa (powder drink mix); ultra manzana lax powder (powder drink mix) from Api-Royal, S.A de CV can be detained without physical examination under Import Alert 99-39; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectApi-Royal, S.A de C added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.