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Importadora y Manufacturer Bruluart

FDA import alert and refusal historySan Francisco, MexicoFEI 3018998917

Recorded by FDA as IMPORTADORA Y MANUFACTURER BRULUART

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Example subjectImportadora y Manufacturer Bruluar added to Import Alert 16-129 (red list)

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As of October 26, 2026, Importadora y Manufacturer Bruluart is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between April 8, 2022 and July 16, 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 b12 (cyanocobalamin) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Importadora y Manufacturer Bruluart

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

2024

  1. Import refusal
    Refused, Vitamin b12 (cyanocobalamin)UNAPPROVEDEntry 799-1456347-4
    Source

2022

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 799-0711324-5
    Source
  2. Import refusal
    Refused, Vitamin b12 (cyanocobalamin)UNAPPROVEDEntry 799-7552681-4
    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 Importadora y Manufacturer Bruluart

Is Importadora y Manufacturer Bruluart on an FDA import alert?
No listing for Importadora y Manufacturer Bruluart 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 Importadora y Manufacturer Bruluart?
Yes. FDA refused 3 shipment lines from Importadora y Manufacturer Bruluart between April 8, 2022 and July 16, 2024. The most recent, on July 16, 2024, was vitamin b12 (cyanocobalamin), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Importadora y Manufacturer Bruluart's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 3 lines).
What is Importadora y Manufacturer Bruluart's FEI number?
Importadora y Manufacturer Bruluart's FDA Establishment Identifier (FEI) is 3018998917.

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Example subjectImportadora y Manufacturer Bruluar added to Import Alert 16-129 (red list)

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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.