SupplierRadar
Sign inStart free

TECNOFARMA S.A. de C.V

FDA import alert and refusal historySan Juan Del Rio, MexicoFEI 3012279910

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on TECNOFARMA S.A. de C.V.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectTECNOFARMA S.A. de C. added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 25, 2026, TECNOFARMA S.A. de C.V is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between June 19, 2019 and September 24, 2025, 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 b12 (cyanocobalamin) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for TECNOFARMA S.A. de C.V

3 records, newest first. Each line links to the FDA page it came from.

2025

  1. Import refusal
    Refused, Vitamin b12 (cyanocobalamin)UNAPPROVEDEntry AEK-7451444-7
    Source

2020

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 799-7617300-3
    Source

2019

  1. Import refusal
    Refused, Vitamin b12 (cyanocobalamin)UNAPPROVEDEntry 799-1939296-7
    Source

Refusal charges, in plain English

  • UNAPPROVED3 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.

Questions about TECNOFARMA S.A. de C.V

Is TECNOFARMA S.A. de C.V on an FDA import alert?
No listing for TECNOFARMA S.A. de C.V appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
Has FDA refused shipments from TECNOFARMA S.A. de C.V?
Yes. FDA refused 3 shipment lines from TECNOFARMA S.A. de C.V between June 19, 2019 and September 24, 2025. The most recent, on September 24, 2025, was vitamin b12 (cyanocobalamin), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse TECNOFARMA S.A. de C.V's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 3 lines).
What is TECNOFARMA S.A. de C.V's FEI number?
TECNOFARMA S.A. de C.V's FDA Establishment Identifier (FEI) is 3012279910.

Buying from TECNOFARMA S.A. de C.V?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on TECNOFARMA S.A. de C.V.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectTECNOFARMA S.A. de C. added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

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.