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Green Product Dooel

FDA import alert and refusal historyTetovo, North MacedoniaFEI 3009048072

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Example subjectGreen Product Dooe added to Import Alert 16-129 (red list)

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As of October 26, 2026, Green Product Dooel (Tetovo, North Macedonia) is on the red list of FDA Import Alert 99-38 (Low-acid canned/acidified foods: inadequate process control) for whole grains/milled grain products/starches; bakery products/dough/mixes/icings; macaroni/noodle products; cereal preparations/breakfast foods; snack food items; milk/butter/dried milk products; cheese/cheese products; ice cream and related products; filled milk/imitation milk products; eggs/egg pr…, published by FDA on May 8, 2015, and has 28 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Catsup · INADPRCCTL
Last warning letter
None found
Last inspection
Classified OAI (Official Action Indicated)

Every FDA record for Green Product Dooel

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

2024

  1. Import refusal
    Refused, 28 lines in one entry: Catsup; Pepper, hot, dried or paste and 6 moreINADPRCCTLNO PROCESSEntry 073-0119279-0Show 28 lines
    Source

2015

  1. Import alert listing
    Listed on Import Alert 99-38red listWhole Grains/Milled Grain Products/Starches; Bakery Products/Dough/Mixes/Icings; Macaroni/Noodle Products; Cereal Preparations/Breakfast Foods; Snack Food Items; Milk/Butter/Dried Milk Products; Cheese/Cheese Products; Ice Cream and related Products; Filled Milk/Imitation Milk Products; Eggs/Egg Pr…
    Source
  2. Inspection
    Inspection classified OAI (Official Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • INADPRCCTL28 refused lines

    Inadequate process controls

    The product appeared to have been prepared, packed, or held under insanitary conditions because of inadequate process controls, whereby it may have become contaminated or injurious to health.

  • NO PROCESS28 refused lines

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about Green Product Dooel

Is Green Product Dooel on an FDA import alert?
Yes. As of October 26, 2026, Green Product Dooel is on the red list of FDA Import Alert 99-38, “Low-acid canned/acidified foods: inadequate process control”, for whole grains/milled grain products/starches; bakery products/dough/mixes/icings; macaroni/noodle products; cereal preparations/breakfast foods; snack food items; milk/butter/dried milk products; cheese/cheese products; ice cream and related products; filled milk/imitation milk products; eggs/egg pr…; FDA published the listing on May 8, 2015.
Has FDA refused shipments from Green Product Dooel?
Yes. FDA refused 28 shipment lines from Green Product Dooel on May 6, 2024. The most recent, on May 6, 2024, was catsup, charged as INADPRCCTL (inadequate process controls).
Why did FDA refuse Green Product Dooel's shipments?
The most frequent charges are INADPRCCTL (inadequate process controls, 28 lines) and NO PROCESS (no scheduled process filed, 28 lines).
When was Green Product Dooel last inspected by FDA?
FDA's most recent inspection of Green Product Dooel with a final classification is dated February 11, 2015 and was classified OAI (Official Action Indicated).
What is Green Product Dooel's FEI number?
Green Product Dooel's FDA Establishment Identifier (FEI) is 3009048072.
Can shipments from Green Product Dooel still enter the U.S.?
Shipments of whole grains/milled grain products/starches; bakery products/dough/mixes/icings; macaroni/noodle products; cereal preparations/breakfast foods; snack food items; milk/butter/dried milk products; cheese/cheese products; ice cream and related products; filled milk/imitation milk products; eggs/egg pr… from Green Product Dooel can be detained without physical examination under Import Alert 99-38; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectGreen Product Dooe 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.