Wonil Food. Co., Ltd.
FDA import alert and refusal historyJingcheon-gun, South KoreaFEI 3003355383
As of October 26, 2026, Wonil Food. Co., Ltd. (Jingcheon-gun, South Korea) is on the red list of FDA Import Alert 99-38 (Low-acid canned/acidified foods: inadequate process control) for mabo tofu sauce, published by FDA on June 3, 2014, 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 99-38 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Wonil Food. Co., Ltd.
3 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2014
- Import alert listingListed on Import Alert 99-38red listMabo Tofu SauceSource
2013
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Wonil Food. Co., Ltd.
- Is Wonil Food. Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Wonil Food. Co., Ltd. is on the red list of FDA Import Alert 99-38, “Low-acid canned/acidified foods: inadequate process control”, for mabo tofu sauce; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from Wonil Food. Co., Ltd.?
- No FDA import refusals for Wonil Food. Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Wonil Food. Co., Ltd. last inspected by FDA?
- FDA's most recent inspection of Wonil Food. Co., Ltd. with a final classification is dated October 18, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Wonil Food. Co., Ltd.'s FEI number?
- Wonil Food. Co., Ltd.'s FDA Establishment Identifier (FEI) is 3003355383.
- Can shipments from Wonil Food. Co., Ltd. still enter the U.S.?
- Shipments of mabo tofu sauce from Wonil Food. Co., Ltd. can be detained without physical examination under Import Alert 99-38; 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.