Gen Food
FDA import alert and refusal historyYangsan-si, South KoreaFEI 3010012806
Recorded by FDA as GEN FOOD
As of October 26, 2026, Gen Food (Yangsan-si, South Korea) is on the red list of FDA Import Alert 99-37 (Low-acid canned/acidified foods without scheduled process) for soybean sauce for soybean paste bibimbap, published by FDA on February 27, 2020, 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 99-37 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Gen Food
2 records, newest first. Each line links to the FDA page it came from.
2020
- Import alert listingListed on Import Alert 99-37red listSoybean Sauce for Soybean Paste BibimbapSource
2019
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about Gen Food
- Is Gen Food on an FDA import alert?
- Yes. As of October 26, 2026, Gen Food is on the red list of FDA Import Alert 99-37, “Low-acid canned/acidified foods without scheduled process”, for soybean sauce for soybean paste bibimbap; FDA published the listing on February 27, 2020.
- Has FDA refused shipments from Gen Food?
- No FDA import refusals for Gen Food appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Gen Food last inspected by FDA?
- FDA's most recent inspection of Gen Food with a final classification is dated October 15, 2019 and was classified OAI (Official Action Indicated).
- What is Gen Food's FEI number?
- Gen Food's FDA Establishment Identifier (FEI) is 3010012806.
- Can shipments from Gen Food still enter the U.S.?
- Shipments of soybean sauce for soybean paste bibimbap from Gen Food can be detained without physical examination under Import Alert 99-37; 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.