Daeha Food
FDA import alert and refusal historyChungju, South KoreaFEI 2000013471
As of October 25, 2026, Daeha Food (Chungju, South Korea) is on the red list of FDA Import Alert 16-74 (Uneviscerated salt-cured, dried, smoked or fermented fish) for dried anchovy, published by FDA on June 13, 2011, 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 16-74 · red listIA 45-02 · 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 Daeha Food
3 records, newest first. Each line links to the FDA page it came from.
2014
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2011
- Import alert listingListed on Import Alert 16-74red listDried AnchovySource
- Import alert listingListed on Import Alert 45-02red listKorean Cookie Cheesebits CrackersSource
Questions about Daeha Food
- Is Daeha Food on an FDA import alert?
- Yes. As of October 25, 2026, Daeha Food is on the red list of FDA Import Alert 16-74, “Uneviscerated salt-cured, dried, smoked or fermented fish”, for dried anchovy; FDA published the listing on June 13, 2011.
- Has FDA refused shipments from Daeha Food?
- No FDA import refusals for Daeha Food appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Daeha Food last inspected by FDA?
- FDA's most recent inspection of Daeha Food with a final classification is dated March 11, 2014 and was classified VAI (Voluntary Action Indicated).
- What is Daeha Food's FEI number?
- Daeha Food's FDA Establishment Identifier (FEI) is 2000013471.
- Can shipments from Daeha Food still enter the U.S.?
- Shipments of dried anchovy from Daeha Food can be detained without physical examination under Import Alert 16-74; 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.