Areka
FDA import alert and refusal historyGuerville, FranceFEI 3001050994
As of October 25, 2026, Areka is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on January 18, 2018, most often for required label information not in english (NO ENGLISH).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Mint candy, hard, without nuts and fruit (without chocolate) · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Areka
3 records, newest first. Each line links to the FDA page it came from.
2018
- Import refusalSource
Refused, 2 lines in one entry: Mint candy, hard, without nuts and fruit (without chocolate)NO ENGLISHEntry UPS-6695391-1Show 2 linesHide lines
- Refused, Mint candy, hard, without nuts and fruit (without chocolate)NO ENGLISHEntry UPS-6695391-1Source
- Refused, Mint candy, hard, without nuts and fruit (without chocolate)NO ENGLISHEntry UPS-6695391-1Source
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Refusal charges, in plain English
- NO ENGLISH2 refused lines
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
Questions about Areka
- Is Areka on an FDA import alert?
- No listing for Areka 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 Areka?
- Yes. FDA refused 2 shipment lines from Areka on January 18, 2018. The most recent, on January 18, 2018, was mint candy, hard, without nuts and fruit (without chocolate), charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Areka's shipments?
- The most frequent charge is NO ENGLISH (required label information not in english, 2 lines).
- When was Areka last inspected by FDA?
- FDA's most recent inspection of Areka with a final classification is dated February 22, 2016 and was classified VAI (Voluntary Action Indicated).
- What is Areka's FEI number?
- Areka's FDA Establishment Identifier (FEI) is 3001050994.
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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.