Is Vibamex Infusiones y Te, SA de CV on an FDA import alert?

No listing for Vibamex Infusiones y Te, SA de CV 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 Vibamex Infusiones y Te, SA de CV?

Yes. FDA refused 2 shipment lines from Vibamex Infusiones y Te, SA de CV on November 20, 2017. The most recent, on November 20, 2017, was mixed fruit, dried or paste, n.e.c.,, charged as SULFITELBL (sulfitelbl).

Why did FDA refuse Vibamex Infusiones y Te, SA de CV's shipments?

The most frequent charges are FALSE (false or misleading labeling, 2 lines) and SULFITELBL (sulfitelbl, 2 lines).

When was Vibamex Infusiones y Te, SA de CV last inspected by FDA?

FDA's most recent inspection of Vibamex Infusiones y Te, SA de CV with a final classification is dated May 16, 2019 and was classified NAI (No Action Indicated).

What is Vibamex Infusiones y Te, SA de CV's FEI number?

Vibamex Infusiones y Te, SA de CV's FDA Establishment Identifier (FEI) is 3013866004.

Vibamex Infusiones y Te, SA de CV

FDA import alert and refusal historyZapopan, MexicoFEI 3013866004

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As of October 26, 2026, Vibamex Infusiones y Te, SA de CV is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on November 20, 2017, most often for false or misleading labeling (FALSE).

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: Nov 20, 2017Mixed fruit, dried or paste, n.e.c., · SULFITELBL
Last warning letter: None found
Last inspection: May 16, 2019Classified NAI (No Action Indicated)

Every FDA record for Vibamex Infusiones y Te, SA de CV

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

2019

May 16, 2019Inspection
Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
Source

2017

Nov 20, 2017Import refusal
Refused, 2 lines in one entry: Mixed fruit, dried or paste, n.e.c.,SULFITELBLFALSEEntry 92F-0008493-0Show 2 linesHide lines
- Refused, Mixed fruit, dried or paste, n.e.c.,SULFITELBL FALSEEntry 92F-0008493-0Source
- Refused, Mixed fruit, dried or paste, n.e.c.,SULFITELBL FALSEEntry 92F-0008493-0Source
Source

Refusal charges, in plain English

FALSE2 refused lines
False or misleading labeling
The labeling appeared to be false or misleading in some particular.
SULFITELBL2 refused lines
SULFITELBL

Questions about Vibamex Infusiones y Te, SA de CV

Is Vibamex Infusiones y Te, SA de CV on an FDA import alert?: No listing for Vibamex Infusiones y Te, SA de CV 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 Vibamex Infusiones y Te, SA de CV?: Yes. FDA refused 2 shipment lines from Vibamex Infusiones y Te, SA de CV on November 20, 2017. The most recent, on November 20, 2017, was mixed fruit, dried or paste, n.e.c.,, charged as SULFITELBL (sulfitelbl).
Why did FDA refuse Vibamex Infusiones y Te, SA de CV's shipments?: The most frequent charges are FALSE (false or misleading labeling, 2 lines) and SULFITELBL (sulfitelbl, 2 lines).
When was Vibamex Infusiones y Te, SA de CV last inspected by FDA?: FDA's most recent inspection of Vibamex Infusiones y Te, SA de CV with a final classification is dated May 16, 2019 and was classified NAI (No Action Indicated).
What is Vibamex Infusiones y Te, SA de CV's FEI number?: Vibamex Infusiones y Te, SA de CV's FDA Establishment Identifier (FEI) is 3013866004.

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