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
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
- Import alerts
- IA 99-39 · red list
- 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
- Import alert listingListed 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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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.