Admichonta S.A.
FDA import alert and refusal historySanto Domingo De Onzole, EcuadorFEI 3013190696
Recorded by FDA as ADMICHONTA S.A.
As of October 26, 2026, Admichonta S.A. (Santo Domingo De Onzole, Ecuador) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh eddoes, published by FDA on May 4, 2018, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-05 · red list
- Last import refusal
- Taro, dasheen (root & tuber vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Admichonta S.A.
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE2 refused lines
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about Admichonta S.A.
- Is Admichonta S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Admichonta S.A. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh eddoes; FDA published the listing on May 4, 2018.
- Has FDA refused shipments from Admichonta S.A.?
- Yes. FDA refused 2 shipment lines from Admichonta S.A. between April 30, 2018 and May 13, 2021. The most recent, on May 13, 2021, was taro, dasheen (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Admichonta S.A.'s shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Admichonta S.A.'s FEI number?
- Admichonta S.A.'s FDA Establishment Identifier (FEI) is 3013190696.
- Can shipments from Admichonta S.A. still enter the U.S.?
- Shipments of fresh eddoes from Admichonta S.A. can be detained without physical examination under Import Alert 99-05; 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.