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globe overseas inc.

FDA import alert and refusal historyJalandhar City, IndiaFEI 3016663161

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Example subjectglobe overseas inc added to Import Alert 16-129 (red list)

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As of October 26, 2026, globe overseas inc. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on December 15, 2023, most often for pesticide chemical residue (PESTICIDE).

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

Current status

Import alerts
Not listed
Last import refusal
Soy fiber (meat extenders) · PESTICIDE
Last warning letter
None found
Last inspection
None on record

Every FDA record for globe overseas inc.

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

2023

  1. Import refusal
    Refused, Soy fiber (meat extenders)PESTICIDEEntry 9PM-2666844-4
    Source

Refusal charges, in plain English

  • PESTICIDE1 refused line

    Pesticide chemical residue

    The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

Questions about globe overseas inc.

Is globe overseas inc. on an FDA import alert?
No listing for globe overseas inc. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
Has FDA refused shipments from globe overseas inc.?
Yes. FDA refused 1 shipment line from globe overseas inc. on December 15, 2023. The most recent, on December 15, 2023, was soy fiber (meat extenders), charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse globe overseas inc.'s shipments?
The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
What is globe overseas inc.'s FEI number?
globe overseas inc.'s FDA Establishment Identifier (FEI) is 3016663161.

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Example subjectglobe overseas inc 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.