Chiles Secos Andrade, S.A. De C.V.
FDA import alert and refusal historyHermosillo, MexicoFEI 3000257133
As of October 26, 2026, Chiles Secos Andrade, S.A. De C.V. is on the green list of FDA Import Alert 24-11, which exempts its listed products from detention without physical examination under that alert, 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 24-11 · green list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Chiles Secos Andrade, S.A. De C.V.
2 records, newest first. Each line links to the FDA page it came from.
2010
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 24-11green listAll Dried Peppers; Pepper, Hot, N.E.C. (Fruit Used as Vegetable); Pepper, Hot, Dried or PasteSource
Questions about Chiles Secos Andrade, S.A. De C.V.
- Is Chiles Secos Andrade, S.A. De C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Chiles Secos Andrade, S.A. De C.V. is on the green list of FDA Import Alert 24-11, “Dried peppers from Mexico”, for all dried peppers; pepper, hot, n.e.c. (fruit used as vegetable); pepper, hot, dried or paste; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Chiles Secos Andrade, S.A. De C.V.?
- No FDA import refusals for Chiles Secos Andrade, S.A. De C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Chiles Secos Andrade, S.A. De C.V. last inspected by FDA?
- FDA's most recent inspection of Chiles Secos Andrade, S.A. De C.V. with a final classification is dated December 3, 2010 and was classified NAI (No Action Indicated).
- What is Chiles Secos Andrade, S.A. De C.V.'s FEI number?
- Chiles Secos Andrade, S.A. De C.V.'s FDA Establishment Identifier (FEI) is 3000257133.
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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.