txiki ltda
FDA import alert and refusal historySan Fernando, ChileFEI 3007991814
As of October 26, 2026, txiki ltda (San Fernando, Chile) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for grapes, published by FDA on June 22, 2018, and has 1 FDA import refusal 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
- Grapes (berry) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for txiki ltda
2 records, newest first. Each line links to the FDA page it came from.
2018
- Import refusalRefused, Grapes (berry)PESTICIDEEntry 97E-0157175-2Source
- Import alert listingListed on Import Alert 99-05red listGrapesSource
Refusal charges, in plain English
- PESTICIDE1 refused line
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 txiki ltda
- Is txiki ltda on an FDA import alert?
- Yes. As of October 26, 2026, txiki ltda is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for grapes; FDA published the listing on June 22, 2018.
- Has FDA refused shipments from txiki ltda?
- Yes. FDA refused 1 shipment line from txiki ltda on June 26, 2018. The most recent, on June 26, 2018, was grapes (berry), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse txiki ltda's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is txiki ltda's FEI number?
- txiki ltda's FDA Establishment Identifier (FEI) is 3007991814.
- Can shipments from txiki ltda still enter the U.S.?
- Shipments of grapes from txiki ltda 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.