Cp Xp
FDA import alert and refusal historyParis, FranceFEI 3009793505
As of October 26, 2026, Cp Xp is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 11, 2021, 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
- Truffle, fungi products, n.e.c. · NO PROCESS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Cp Xp
1 record, newest first. Each line links to the FDA page it came from.
2021
- Import refusalRefused, Truffle, fungi products, n.e.c.NO PROCESSEntry SCS-3626659-3Source
Refusal charges, in plain English
- NO PROCESS1 refused line
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 Cp Xp
- Is Cp Xp on an FDA import alert?
- No listing for Cp Xp 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 Cp Xp?
- Yes. FDA refused 1 shipment line from Cp Xp on February 11, 2021. The most recent, on February 11, 2021, was truffle, fungi products, n.e.c., charged as NO PROCESS (no scheduled process filed).
- Why did FDA refuse Cp Xp's shipments?
- The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
- What is Cp Xp's FEI number?
- Cp Xp's FDA Establishment Identifier (FEI) is 3009793505.
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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.