Regals du Touquet
FDA import alert and refusal historyLe Touquet Paris Plage, FranceFEI 3007985817
Recorded by FDA as REGALS DU TOUQUET
As of October 26, 2026, Regals du Touquet is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 14, 2017, most often for af-nonrsp (AF-NONRSP).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Fish chowder/soup/stew/bisque, mixed fishery/seafood products · AF-NONRSP
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Regals du Touquet
3 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2017
Refusal charges, in plain English
- AF-NONRSP1 refused line
AF-NONRSP
Questions about Regals du Touquet
- Is Regals du Touquet on an FDA import alert?
- No listing for Regals du Touquet appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the France page.
- Has FDA refused shipments from Regals du Touquet?
- Yes. FDA refused 1 shipment line from Regals du Touquet on November 14, 2017. The most recent, on November 14, 2017, was fish chowder/soup/stew/bisque, mixed fishery/seafood products, charged as AF-NONRSP (af-nonrsp).
- Why did FDA refuse Regals du Touquet's shipments?
- The most frequent charge is AF-NONRSP (af-nonrsp, 1 line).
- When was Regals du Touquet last inspected by FDA?
- FDA's most recent inspection of Regals du Touquet with a final classification is dated September 20, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Regals du Touquet's FEI number?
- Regals du Touquet's FDA Establishment Identifier (FEI) is 3007985817.
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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.