Jeong Won Industrial Co.
FDA import alert and refusal historyBoseong, South KoreaFEI 3023463211
As of October 26, 2026, Jeong Won Industrial Co. (Boseong, South Korea) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for mixed grains (mixed cereal); sprouted black rice, published by FDA on September 16, 2009, 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Jeong Won Industrial Co.
2 records, newest first. Each line links to the FDA page it came from.
2023
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 99-08red listMixed Grains (Mixed Cereal); sprouted black riceSource
Questions about Jeong Won Industrial Co.
- Is Jeong Won Industrial Co. on an FDA import alert?
- Yes. As of October 26, 2026, Jeong Won Industrial Co. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for mixed grains (mixed cereal); sprouted black rice; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Jeong Won Industrial Co.?
- No FDA import refusals for Jeong Won Industrial Co. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Jeong Won Industrial Co. last inspected by FDA?
- FDA's most recent inspection of Jeong Won Industrial Co. with a final classification is dated May 12, 2023 and was classified NAI (No Action Indicated).
- What is Jeong Won Industrial Co.'s FEI number?
- Jeong Won Industrial Co.'s FDA Establishment Identifier (FEI) is 3023463211.
- Can shipments from Jeong Won Industrial Co. still enter the U.S.?
- Shipments of mixed grains (mixed cereal); sprouted black rice from Jeong Won Industrial Co. can be detained without physical examination under Import Alert 99-08; 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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