Grupo Alinorsa S.A. de C.V
FDA import alert and refusal historyMonterrey, MexicoFEI 2000029346
As of October 26, 2026, Grupo Alinorsa S.A. de C.V (Monterrey, Mexico) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for tlaquemada sauce; red sauce (salsa), 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Grupo Alinorsa 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 99-08red listTlaquemada sauce; red sauce (Salsa)Source
Questions about Grupo Alinorsa S.A. de C.V
- Is Grupo Alinorsa S.A. de C.V on an FDA import alert?
- Yes. As of October 26, 2026, Grupo Alinorsa S.A. de C.V is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for tlaquemada sauce; red sauce (salsa); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Grupo Alinorsa S.A. de C.V?
- No FDA import refusals for Grupo Alinorsa S.A. de C.V appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Grupo Alinorsa S.A. de C.V's FEI number?
- Grupo Alinorsa S.A. de C.V's FDA Establishment Identifier (FEI) is 2000029346.
- Can shipments from Grupo Alinorsa S.A. de C.V still enter the U.S.?
- Shipments of tlaquemada sauce; red sauce (salsa) from Grupo Alinorsa S.A. de C.V can be detained without physical examination under Import Alert 99-08; 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).
Buying from Grupo Alinorsa S.A. de C.V?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.