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Duga Komerc

FDA import alert and refusal historyKrusevac, SerbiaFEI 3012597446

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Example subjectDuga Komer added to Import Alert 16-129 (red list)

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As of October 25, 2026, Duga Komerc is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on November 15, 2016, most often for nutrition information missing from label (NUTRIT LBL).

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

Current status

Import alerts
Not listed
Last import refusal
Bottled water with fruit flavors, noncarbonated (nonmedicinal) · VITAMN LBL
Last warning letter
None found
Last inspection
None on record

Every FDA record for Duga Komerc

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

2016

  1. Import refusal
    Refused, 3 lines in one entry: Bottled water with fruit flavors, noncarbonated (nonmedicinal)VITAMN LBLNUTRIT LBLEntry EVJ-0176453-2Show 3 lines
    Source

Refusal charges, in plain English

  • NUTRIT LBL3 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.

  • VITAMN LBL3 refused lines

    VITAMN LBL

Questions about Duga Komerc

Is Duga Komerc on an FDA import alert?
No listing for Duga Komerc appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Serbia page.
Has FDA refused shipments from Duga Komerc?
Yes. FDA refused 3 shipment lines from Duga Komerc on November 15, 2016. The most recent, on November 15, 2016, was bottled water with fruit flavors, noncarbonated (nonmedicinal), charged as VITAMN LBL (vitamn lbl).
Why did FDA refuse Duga Komerc's shipments?
The most frequent charges are NUTRIT LBL (nutrition information missing from label, 3 lines) and VITAMN LBL (vitamn lbl, 3 lines).
What is Duga Komerc's FEI number?
Duga Komerc's FDA Establishment Identifier (FEI) is 3012597446.

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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.