Sanofi-Aventis De Mexico
FDA import alert and refusal historyOcoyoacac, MexicoFEI 3008274551
As of October 26, 2026, Sanofi-Aventis De Mexico is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between October 5, 2022 and September 27, 2024, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin c (ascorbic acid) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Sanofi-Aventis De Mexico
3 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalRefused, Vitamin c (ascorbic acid)UNAPPROVEDEntry AEK-5502822-7Source
2022
- Import refusalSource
Refused, 2 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO ENGLISHUNAPPROVEDEntry 799-0711324-5Show 2 linesHide lines
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO ENGLISHEntry 799-0711324-5Source
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 799-0711324-5Source
Refusal charges, in plain English
- UNAPPROVED2 refused lines
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
- 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 Sanofi-Aventis De Mexico
- Is Sanofi-Aventis De Mexico on an FDA import alert?
- No listing for Sanofi-Aventis De Mexico 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 Sanofi-Aventis De Mexico?
- Yes. FDA refused 3 shipment lines from Sanofi-Aventis De Mexico between October 5, 2022 and September 27, 2024. The most recent, on September 27, 2024, was vitamin c (ascorbic acid), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Sanofi-Aventis De Mexico's shipments?
- The most frequent charges are UNAPPROVED (unapproved new drug, 2 lines) and NO ENGLISH (required label information not in english, 1 line).
- What is Sanofi-Aventis De Mexico's FEI number?
- Sanofi-Aventis De Mexico's FDA Establishment Identifier (FEI) is 3008274551.
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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.