Ceosa,SA de CV
FDA import alert and refusal historyOrizaba, MexicoFEI 3017123336
Recorded by FDA as CEOSA,SA DE CV
As of October 26, 2026, Ceosa,SA de CV is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 1, 2026, most often for major food allergen not declared (ALLERGEN).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Sauces, n.e.c. · ALLERGEN
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ceosa,SA de CV
1 record, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Sauces, n.e.c.ALLERGENNO PROCESSEntry BJG-0210895-8Source
Refusal charges, in plain English
- ALLERGEN1 refused line
Major food allergen not declared
The label appeared not to declare all major food allergens present in the product, as section 403(w) of the FD&C Act requires.
- 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 Ceosa,SA de CV
- Is Ceosa,SA de CV on an FDA import alert?
- No listing for Ceosa,SA de CV appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
- Has FDA refused shipments from Ceosa,SA de CV?
- Yes. FDA refused 1 shipment line from Ceosa,SA de CV on May 1, 2026. The most recent, on May 1, 2026, was sauces, n.e.c., charged as ALLERGEN (major food allergen not declared).
- Why did FDA refuse Ceosa,SA de CV's shipments?
- The most frequent charges are ALLERGEN (major food allergen not declared, 1 line) and NO PROCESS (no scheduled process filed, 1 line).
- What is Ceosa,SA de CV's FEI number?
- Ceosa,SA de CV's FDA Establishment Identifier (FEI) is 3017123336.
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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.