Firmenich De Mexico S.A. De C.V.
FDA import alert and refusal historyToluca, MexicoFEI 3002988985
As of October 26, 2026, Firmenich De Mexico S.A. De C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 3, 2017, most often for ingredients not listed (LIST INGRE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Flavoring agents and adjuvants (food additives for human use) · LIST INGRE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Firmenich De Mexico S.A. De C.V.
1 record, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Flavoring agents and adjuvants (food additives for human use)LIST INGREEntry 336-2690595-9Source
Refusal charges, in plain English
- LIST INGRE1 refused line
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
Questions about Firmenich De Mexico S.A. De C.V.
- Is Firmenich De Mexico S.A. De C.V. on an FDA import alert?
- No listing for Firmenich De Mexico S.A. De C.V. 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 Firmenich De Mexico S.A. De C.V.?
- Yes. FDA refused 1 shipment line from Firmenich De Mexico S.A. De C.V. on March 3, 2017. The most recent, on March 3, 2017, was flavoring agents and adjuvants (food additives for human use), charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Firmenich De Mexico S.A. De C.V.'s shipments?
- The most frequent charge is LIST INGRE (ingredients not listed, 1 line).
- What is Firmenich De Mexico S.A. De C.V.'s FEI number?
- Firmenich De Mexico S.A. De C.V.'s FDA Establishment Identifier (FEI) is 3002988985.
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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.