Onetik
FDA import alert and refusal historyMacaye, FranceFEI 3004265685
Recorded by FDA as ONETIK
As of October 26, 2026, Onetik is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 4, 2024, most often for listeria monocytogenes (LISTERIA).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Soft ripened cheese made from goat's milk (e.g., chevre, feta, goat) · LISTERIA
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Onetik
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- LISTERIA1 refused line
Listeria monocytogenes
The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Onetik
- Is Onetik on an FDA import alert?
- No listing for Onetik 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 Onetik?
- Yes. FDA refused 1 shipment line from Onetik on October 4, 2024. The most recent, on October 4, 2024, was soft ripened cheese made from goat's milk (e.g., chevre, feta, goat), charged as LISTERIA (listeria monocytogenes).
- Why did FDA refuse Onetik's shipments?
- The most frequent charge is LISTERIA (listeria monocytogenes, 1 line).
- When was Onetik last inspected by FDA?
- FDA's most recent inspection of Onetik with a final classification is dated February 17, 2015 and was classified NAI (No Action Indicated).
- What is Onetik's FEI number?
- Onetik's FDA Establishment Identifier (FEI) is 3004265685.
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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.