Iriada International Limited
FDA import alert and refusal historySankt-Peterburg, RussiaFEI 3007915563
As of October 26, 2026, Iriada International Limited (Sankt-Peterburg, Russia) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for soft candy (marmalade), published by FDA on October 2, 2015, is also listed on Import Alert 45-02 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red listIA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Iriada International Limited
2 records, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-39red listSoft Candy (Marmalade)Source
2011
- Import alert listingListed on Import Alert 45-02red listSharmel Zephyr in Chocolate with Ice Cream Taste (Cookies); Soft Candy (Marmalade); Dragee-Morskee Kamushki (Candy)Source
Questions about Iriada International Limited
- Is Iriada International Limited on an FDA import alert?
- Yes. As of October 26, 2026, Iriada International Limited is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for soft candy (marmalade); FDA published the listing on October 2, 2015.
- Has FDA refused shipments from Iriada International Limited?
- No FDA import refusals for Iriada International Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Iriada International Limited's FEI number?
- Iriada International Limited's FDA Establishment Identifier (FEI) is 3007915563.
- Can shipments from Iriada International Limited still enter the U.S.?
- Shipments of soft candy (marmalade) from Iriada International Limited can be detained without physical examination under Import Alert 99-39; 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.