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Ioannis Nenoglou kai SIA EE

FDA import alert and refusal historyKilkis, GreeceFEI 3016665369

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Example subjectIoannis Nenoglou kai SIA E added to Import Alert 16-129 (red list)

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As of October 26, 2026, Ioannis Nenoglou kai SIA EE is not on any FDA import alert in SupplierRadar's records; FDA refused 12 of its shipment lines between September 29, 2021 and April 8, 2022, most often for unapproved new drug (UNAPPROVED).

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

Current status

Import alerts
Not listed
Last import refusal
Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · LIST INGRE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Ioannis Nenoglou kai SIA EE

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

2022

  1. Import refusal
    Refused, 3 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LIST INGRENUTRIT LBLUNAPPROVEDEntry 799-7821266-9Show 3 lines
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LIST INGRENUTRIT LBLEntry 799-7821266-9Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 799-7821266-9Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LIST INGRENUTRIT LBLEntry 799-7821266-9Source
    Source
  2. Import refusal
    Refused, 4 lines in one entry: Chlorella (tablet), vit/min/protein/unconventional dietary spec for human/animal, n.e.c.)LIST INGRENUTRIT LBLUNAPPROVEDEntry 799-6487159-3Show 4 lines
    Source

2021

  1. Import refusal
    Refused, 5 lines in one entry: Herbals & botanicals (not teas), n.e.c.NCONTACTUNAPPROVEDEntry 799-4638958-1Show 5 lines
    Source

Refusal charges, in plain English

  • UNAPPROVED10 refused lines

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

  • LIST INGRE6 refused lines

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

  • NUTRIT LBL6 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.

  • NCONTACT5 refused lines

    No U.S. adverse event contact on supplement label

    The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

Questions about Ioannis Nenoglou kai SIA EE

Is Ioannis Nenoglou kai SIA EE on an FDA import alert?
No listing for Ioannis Nenoglou kai SIA EE appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Greece page.
Has FDA refused shipments from Ioannis Nenoglou kai SIA EE?
Yes. FDA refused 12 shipment lines from Ioannis Nenoglou kai SIA EE between September 29, 2021 and April 8, 2022. The most recent, on April 8, 2022, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as LIST INGRE (ingredients not listed).
Why did FDA refuse Ioannis Nenoglou kai SIA EE's shipments?
The most frequent charges are UNAPPROVED (unapproved new drug, 10 lines) and LIST INGRE (ingredients not listed, 6 lines).
What is Ioannis Nenoglou kai SIA EE's FEI number?
Ioannis Nenoglou kai SIA EE's FDA Establishment Identifier (FEI) is 3016665369.

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Example subjectIoannis Nenoglou kai SIA E 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.