Verges Gascogne
FDA import alert and refusal historyMontestru Sur, FranceFEI 3003729640
As of October 25, 2026, Verges Gascogne is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on June 28, 2017, most often for no scheduled process filed (NO PROCESS).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Apricot (pit fruit) · NO PROCESS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Verges Gascogne
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalSource
Refused, 2 lines in one entry: Apricot (pit fruit); Pear (core fruit)NO PROCESSEntry 231-6768427-7Show 2 linesHide lines
- Refused, Apricot (pit fruit)NO PROCESSEntry 231-6768427-7Source
- Refused, Pear (core fruit)NO PROCESSEntry 231-6768427-7Source
Refusal charges, in plain English
- NO PROCESS2 refused lines
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
Questions about Verges Gascogne
- Is Verges Gascogne on an FDA import alert?
- No listing for Verges Gascogne appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the France page.
- Has FDA refused shipments from Verges Gascogne?
- Yes. FDA refused 2 shipment lines from Verges Gascogne on June 28, 2017. The most recent, on June 28, 2017, was apricot (pit fruit), charged as NO PROCESS (no scheduled process filed).
- Why did FDA refuse Verges Gascogne's shipments?
- The most frequent charge is NO PROCESS (no scheduled process filed, 2 lines).
- What is Verges Gascogne's FEI number?
- Verges Gascogne's FDA Establishment Identifier (FEI) is 3003729640.
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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.