Sodifer S.A.
FDA import alert and refusal historyLisbon, PortugalFEI 3012532432
Recorded by FDA as SODIFER S.A.
As of October 26, 2026, Sodifer S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on July 19, 2017, most often for artificial coloring not declared (COLOR LBLG).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Icing and icing mixes without chocolate or nuts · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Sodifer S.A.
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalSource
Refused, 2 lines in one entry: Icing and icing mixes without chocolate or nutsUNSAFE COLCOLOR LBLGEntry 101-5494479-7Show 2 linesHide lines
- Refused, Icing and icing mixes without chocolate or nutsUNSAFE COLCOLOR LBLGEntry 101-5494479-7Source
- Refused, Icing and icing mixes without chocolate or nutsUNSAFE COLCOLOR LBLGEntry 101-5494479-7Source
Refusal charges, in plain English
- COLOR LBLG2 refused lines
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- UNSAFE COL2 refused lines
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about Sodifer S.A.
- Is Sodifer S.A. on an FDA import alert?
- No listing for Sodifer S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Portugal page.
- Has FDA refused shipments from Sodifer S.A.?
- Yes. FDA refused 2 shipment lines from Sodifer S.A. on July 19, 2017. The most recent, on July 19, 2017, was icing and icing mixes without chocolate or nuts, charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Sodifer S.A.'s shipments?
- The most frequent charges are COLOR LBLG (artificial coloring not declared, 2 lines) and UNSAFE COL (color additive unsafe under section 721, 2 lines).
- What is Sodifer S.A.'s FEI number?
- Sodifer S.A.'s FDA Establishment Identifier (FEI) is 3012532432.
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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.