Koro Company
FDA import alert and refusal historySkopje, North MacedoniaFEI 3010133793
As of October 26, 2026, Koro Company (Skopje, North Macedonia) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for camomile flowers, published by FDA on October 8, 2021, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-19 · red list
- Last import refusal
- Tea, camomille, chamomile (tea substitute) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Koro Company
2 records, newest first. Each line links to the FDA page it came from.
2022
- Import refusalRefused, Tea, camomille, chamomile (tea substitute)SALMONELLAEntry 071-0246056-0Source
2021
- Import alert listingListed on Import Alert 99-19red listCamomile FlowersSource
Refusal charges, in plain English
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Koro Company
- Is Koro Company on an FDA import alert?
- Yes. As of October 26, 2026, Koro Company is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for camomile flowers; FDA published the listing on October 8, 2021.
- Has FDA refused shipments from Koro Company?
- Yes. FDA refused 1 shipment line from Koro Company on July 20, 2022. The most recent, on July 20, 2022, was tea, camomille, chamomile (tea substitute), charged as SALMONELLA (salmonella).
- Why did FDA refuse Koro Company's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Koro Company's FEI number?
- Koro Company's FDA Establishment Identifier (FEI) is 3010133793.
- Can shipments from Koro Company still enter the U.S.?
- Shipments of camomile flowers from Koro Company can be detained without physical examination under Import Alert 99-19; 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.