Rojiar (Rojar) Corp. (Manufacturing site)
FDA import alert and refusal historyTehran, IranFEI 3003315479
As of October 26, 2026, Rojiar (Rojar) Corp. (Manufacturing site) (Tehran, Iran) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for watermelon seeds, published by FDA on March 28, 2022, is also listed on Import Alert 99-08 (red list) and Import Alert 99-19 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Rojiar (Rojar) Corp. (Manufacturing site)
3 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 45-02red listWatermelon SeedsSource
2009
- Import alert listingListed on Import Alert 99-08red listdried red datesSource
- Import alert listingListed on Import Alert 99-19red listSoft Candy without Nuts and Fruit, N.E.C. (without Chocolate)Source
Questions about Rojiar (Rojar) Corp. (Manufacturing site)
- Is Rojiar (Rojar) Corp. (Manufacturing site) on an FDA import alert?
- Yes. As of October 26, 2026, Rojiar (Rojar) Corp. (Manufacturing site) is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for watermelon seeds; FDA published the listing on March 28, 2022.
- Has FDA refused shipments from Rojiar (Rojar) Corp. (Manufacturing site)?
- No FDA import refusals for Rojiar (Rojar) Corp. (Manufacturing site) appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Rojiar (Rojar) Corp. (Manufacturing site)'s FEI number?
- Rojiar (Rojar) Corp. (Manufacturing site)'s FDA Establishment Identifier (FEI) is 3003315479.
- Can shipments from Rojiar (Rojar) Corp. (Manufacturing site) still enter the U.S.?
- Shipments of watermelon seeds from Rojiar (Rojar) Corp. (Manufacturing site) can be detained without physical examination under Import Alert 45-02; 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.