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Biofarma Natural CMD S.A. de C.V.

FDA import alert and refusal historyZapopan, MexicoFEI 3009079147

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Example subjectBiofarma Natural CMD S.A. de C.V added to Import Alert 16-129 (red list)

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As of October 26, 2026, Biofarma Natural CMD S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between October 31, 2019 and June 11, 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
Folic acid (vitamin) · UNAPPROVED
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Biofarma Natural CMD S.A. de C.V.

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

2025

  1. Import refusal
    Refused, Folic acid (vitamin)UNAPPROVEDEntry 799-7946192-9
    Source

2024

  1. Import refusal
    Refused, Folic acid (vitamin)UNAPPROVEDEntry 799-1071876-7
    Source
  2. Import refusal
    Refused, Vitamin c (ascorbic acid)NOT LISTEDFRNMFGREGUNAPPROVEDEntry 799-9893612-4
    Source

2019

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 799-3999260-6
    Source

2013

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ
    Source

Refusal charges, in plain English

  • UNAPPROVED4 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.

  • FRNMFGREG1 refused line

    FRNMFGREG

  • NOT LISTED1 refused line

    Product not listed with FDA

    The product appeared to be a drug or device that is not included in the listing FDA requires under section 510(j) of the FD&C Act.

Questions about Biofarma Natural CMD S.A. de C.V.

Is Biofarma Natural CMD S.A. de C.V. on an FDA import alert?
No listing for Biofarma Natural CMD 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 Biofarma Natural CMD S.A. de C.V.?
Yes. FDA refused 4 shipment lines from Biofarma Natural CMD S.A. de C.V. between October 31, 2019 and June 11, 2025. The most recent, on June 11, 2025, was folic acid (vitamin), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Biofarma Natural CMD S.A. de C.V.'s shipments?
The most frequent charges are UNAPPROVED (unapproved new drug, 4 lines) and FRNMFGREG (frnmfgreg, 1 line).
When was Biofarma Natural CMD S.A. de C.V. last inspected by FDA?
FDA's most recent inspection of Biofarma Natural CMD S.A. de C.V. with a final classification is dated April 19, 2013 and was classified NAI (No Action Indicated).
What is Biofarma Natural CMD S.A. de C.V.'s FEI number?
Biofarma Natural CMD S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3009079147.

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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.