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Chocovron Global Corp

FDA import alert and refusal historySan Pedro,Laguna, PhilippinesFEI 3014397812

Recorded by FDA as CHOCOVRON GLOBAL CORP

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Example subjectChocovron Global Cor added to Import Alert 16-129 (red list)

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As of October 26, 2026, Chocovron Global Corp is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 12, 2019, most often for fair packaging and labeling act (LABELING).

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

Current status

Import alerts
Not listed
Last import refusal
Coffee, instant · LABELING
Last warning letter
None found
Last inspection
None on record

Every FDA record for Chocovron Global Corp

1 record, newest first. Each line links to the FDA page it came from.

2019

  1. Import refusal
    Refused, Coffee, instantLABELINGEntry BDD-0677934-8
    Source

Refusal charges, in plain English

  • LABELING1 refused line

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

Questions about Chocovron Global Corp

Is Chocovron Global Corp on an FDA import alert?
No listing for Chocovron Global Corp appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Philippines page.
Has FDA refused shipments from Chocovron Global Corp?
Yes. FDA refused 1 shipment line from Chocovron Global Corp on November 12, 2019. The most recent, on November 12, 2019, was coffee, instant, charged as LABELING (fair packaging and labeling act).
Why did FDA refuse Chocovron Global Corp's shipments?
The most frequent charge is LABELING (fair packaging and labeling act, 1 line).
What is Chocovron Global Corp's FEI number?
Chocovron Global Corp's FDA Establishment Identifier (FEI) is 3014397812.

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Example subjectChocovron Global Cor 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.