Royal Mayan S.A. De C.V.
FDA import alert and refusal historyReynosa, Tamaulipasmexico, MexicoFEI 3000133567
As of October 26, 2026, Royal Mayan S.A. De C.V. (Reynosa, Tamaulipasmexico, Mexico) is on the red list of FDA Import Alert 21-12 (Frozen and refrigerated guacamole and avocado products) for avocado (pit fruit); avocado, dried or paste; guacamole (multiple food specialties, side dishes and desserts), published by FDA on September 16, 2009, 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 21-12 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Royal Mayan S.A. De C.V.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 21-12red listAvocado (Pit Fruit); Avocado, Dried or Paste; Guacamole (Multiple Food Specialties, Side Dishes and Desserts)Source
Questions about Royal Mayan S.A. De C.V.
- Is Royal Mayan S.A. De C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Royal Mayan S.A. De C.V. is on the red list of FDA Import Alert 21-12, “Frozen and refrigerated guacamole and avocado products”, for avocado (pit fruit); avocado, dried or paste; guacamole (multiple food specialties, side dishes and desserts); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Royal Mayan S.A. De C.V.?
- No FDA import refusals for Royal Mayan S.A. De C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Royal Mayan S.A. De C.V.'s FEI number?
- Royal Mayan S.A. De C.V.'s FDA Establishment Identifier (FEI) is 3000133567.
- Can shipments from Royal Mayan S.A. De C.V. still enter the U.S.?
- Shipments of avocado (pit fruit); avocado, dried or paste; guacamole (multiple food specialties, side dishes and desserts) from Royal Mayan S.A. De C.V. can be detained without physical examination under Import Alert 21-12; 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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