Vergo Kwekerijen BVBA
FDA import alert and refusal historyHoogstraten, BelgiumFEI 3011297910
As of October 26, 2026, Vergo Kwekerijen BVBA (Hoogstraten, Belgium) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for red hot finger chilli pepper, published by FDA on August 9, 2016, and has 4 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
- Pepper, hot, n.e.c. (fruit used as vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Vergo Kwekerijen BVBA
6 records, newest first. Each line links to the FDA page it came from.
2019
2018
2017
2016
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
- Import alert listingListed on Import Alert 99-05red listRed Hot Finger Chilli PepperSource
Refusal charges, in plain English
- PESTICIDE4 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 Vergo Kwekerijen BVBA
- Is Vergo Kwekerijen BVBA on an FDA import alert?
- Yes. As of October 26, 2026, Vergo Kwekerijen BVBA is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for red hot finger chilli pepper; FDA published the listing on August 9, 2016.
- Has FDA refused shipments from Vergo Kwekerijen BVBA?
- Yes. FDA refused 4 shipment lines from Vergo Kwekerijen BVBA between May 9, 2017 and February 13, 2019. The most recent, on February 13, 2019, was pepper, hot, n.e.c. (fruit used as vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Vergo Kwekerijen BVBA's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 4 lines).
- When was Vergo Kwekerijen BVBA last inspected by FDA?
- FDA's most recent inspection of Vergo Kwekerijen BVBA with a final classification is dated November 28, 2016 and was classified NAI (No Action Indicated).
- What is Vergo Kwekerijen BVBA's FEI number?
- Vergo Kwekerijen BVBA's FDA Establishment Identifier (FEI) is 3011297910.
- Can shipments from Vergo Kwekerijen BVBA still enter the U.S.?
- Shipments of red hot finger chilli pepper from Vergo Kwekerijen BVBA 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).
Buying from Vergo Kwekerijen BVBA?
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.