Has FDA refused shipments from Eugen Skermo (Morava Honey)?

Yes. FDA refused 4 shipment lines from Eugen Skermo (Morava Honey) between March 17, 2020 and March 18, 2021. The most recent, on March 18, 2021, was honey, charged as UNSAFE ADD (food additive unsafe under section 409).

Why did FDA refuse Eugen Skermo (Morava Honey)'s shipments?

The most frequent charges are VETDRUGRES (animal drug residue, 4 lines) and UNSAFE ADD (food additive unsafe under section 409, 3 lines).

What is Eugen Skermo (Morava Honey)'s FEI number?

Eugen Skermo (Morava Honey)'s FDA Establishment Identifier (FEI) is 3013625489.

Can shipments from Eugen Skermo (Morava Honey) still enter the U.S.?

Shipments of honey from Eugen Skermo (Morava Honey) can be detained without physical examination under Import Alert 36-04; 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).

Eugen Skermo (Morava Honey)

FDA import alert and refusal historyKorce, AlbaniaFEI 3013625489

Recorded by FDA as EUGEN SKERMO (MORAVA HONEY)

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As of October 26, 2026, Eugen Skermo (Morava Honey) (Korce, Albania) is on the red list of FDA Import Alert 36-04 (Honey and blended syrup: drug residues) for honey, published by FDA on March 16, 2020, and has 4 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: IA 36-04 · red list
Last import refusal: Mar 18, 2021Honey · UNSAFE ADD
Last warning letter: None found
Last inspection: None on record

Every FDA record for Eugen Skermo (Morava Honey)

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

2021

Mar 18, 2021Import refusal
Refused, 3 lines in one entry: HoneyUNSAFE ADDVETDRUGRESEntry 9AJ-0821424-7Show 3 linesHide lines
- Refused, HoneyUNSAFE ADD VETDRUGRESEntry 9AJ-0821424-7Source
- Refused, HoneyUNSAFE ADD VETDRUGRESEntry 9AJ-0821424-7Source
- Refused, HoneyUNSAFE ADD VETDRUGRESEntry 9AJ-0821424-7Source
Source

2020

Mar 17, 2020Import refusal
Refused, HoneyVETDRUGRESEntry 9AJ-0816049-9
Source
Mar 16, 2020Import alert listing
Listed on Import Alert 36-04red listHoney
Source

Refusal charges, in plain English

VETDRUGRES4 refused lines
Animal drug residue
The product appeared to contain a new animal drug, or a conversion product of one, that is unsafe within the meaning of section 512 of the FD&C Act.
UNSAFE ADD3 refused lines
Food additive unsafe under section 409
The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

Questions about Eugen Skermo (Morava Honey)

Is Eugen Skermo (Morava Honey) on an FDA import alert?: Yes. As of October 26, 2026, Eugen Skermo (Morava Honey) is on the red list of FDA Import Alert 36-04, “Honey and blended syrup: drug residues”, for honey; FDA published the listing on March 16, 2020.
Has FDA refused shipments from Eugen Skermo (Morava Honey)?: Yes. FDA refused 4 shipment lines from Eugen Skermo (Morava Honey) between March 17, 2020 and March 18, 2021. The most recent, on March 18, 2021, was honey, charged as UNSAFE ADD (food additive unsafe under section 409).
Why did FDA refuse Eugen Skermo (Morava Honey)'s shipments?: The most frequent charges are VETDRUGRES (animal drug residue, 4 lines) and UNSAFE ADD (food additive unsafe under section 409, 3 lines).
What is Eugen Skermo (Morava Honey)'s FEI number?: Eugen Skermo (Morava Honey)'s FDA Establishment Identifier (FEI) is 3013625489.
Can shipments from Eugen Skermo (Morava Honey) still enter the U.S.?: Shipments of honey from Eugen Skermo (Morava Honey) can be detained without physical examination under Import Alert 36-04; 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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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.