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Modhuban

FDA import alert and refusal historyDhaka, BangladeshFEI 3011891212

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As of October 25, 2026, Modhuban is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on December 6, 2016, most often for net quantity statement missing (LACKS N/C).

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

Current status

Import alerts
Not listed
Last import refusal
Plain cookies,biscuits and wafers, n.e.c. · LACKS N/C
Last warning letter
None found
Last inspection
None on record

Every FDA record for Modhuban

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

2016

  1. Import refusal
    Refused, 2 lines in one entry: Plain cookies,biscuits and wafers, n.e.c.LACKS N/CNUTRIT LBLEntry KM6-0088473-8Show 2 lines
    Source

Refusal charges, in plain English

  • LACKS N/C2 refused lines

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

  • NUTRIT LBL2 refused lines

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about Modhuban

Is Modhuban on an FDA import alert?
No listing for Modhuban appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Bangladesh page.
Has FDA refused shipments from Modhuban?
Yes. FDA refused 2 shipment lines from Modhuban on December 6, 2016. The most recent, on December 6, 2016, was plain cookies,biscuits and wafers, n.e.c., charged as LACKS N/C (net quantity statement missing).
Why did FDA refuse Modhuban's shipments?
The most frequent charges are LACKS N/C (net quantity statement missing, 2 lines) and NUTRIT LBL (nutrition information missing from label, 2 lines).
What is Modhuban's FEI number?
Modhuban's FDA Establishment Identifier (FEI) is 3011891212.

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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.