Ferro de Mexico SA de CV
FDA import alert and refusal historyGuadalajara, MexicoFEI 3014329520
Recorded by FDA as FERRO DE MEXICO SA DE CV
As of October 26, 2026, Ferro de Mexico SA de CV is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 7, 2018, most often for imbed objt (IMBED OBJT).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Chocolate candy pieces, without nuts and fruit · IMBED OBJT
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ferro de Mexico SA de CV
1 record, newest first. Each line links to the FDA page it came from.
2018
- Import refusalRefused, Chocolate candy pieces, without nuts and fruitIMBED OBJTNO ENGLISHEntry UPS-8297412-3Source
Refusal charges, in plain English
- IMBED OBJT1 refused line
IMBED OBJT
- NO ENGLISH1 refused line
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 Ferro de Mexico SA de CV
- Is Ferro de Mexico SA de CV on an FDA import alert?
- No listing for Ferro de Mexico 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 Ferro de Mexico SA de CV?
- Yes. FDA refused 1 shipment line from Ferro de Mexico SA de CV on May 7, 2018. The most recent, on May 7, 2018, was chocolate candy pieces, without nuts and fruit, charged as IMBED OBJT (imbed objt).
- Why did FDA refuse Ferro de Mexico SA de CV's shipments?
- The most frequent charges are IMBED OBJT (imbed objt, 1 line) and NO ENGLISH (required label information not in english, 1 line).
- What is Ferro de Mexico SA de CV's FEI number?
- Ferro de Mexico SA de CV's FDA Establishment Identifier (FEI) is 3014329520.
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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.