Otoki Corporation Daepoong Factory
FDA import alert and refusal historyUmseong, South KoreaFEI 3009934446
As of October 26, 2026, Otoki Corporation Daepoong Factory is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between July 10, 2018 and August 28, 2019, most often for no scheduled process filed (NO PROCESS).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · NO PROCESS
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Otoki Corporation Daepoong Factory
7 records, newest first. Each line links to the FDA page it came from.
2019
- Import refusalSource
Refused, 3 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.); Rice, plain (white or polished) processed (packaged)NO PROCESSEntry EJA-5109714-7Show 3 linesHide lines
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)NO PROCESSEntry EJA-5109714-7Source
- Refused, Rice, plain (white or polished) processed (packaged)NO PROCESSEntry EJA-5109714-7Source
- Refused, Rice, plain (white or polished) processed (packaged)NO PROCESSEntry EJA-5109714-7Source
2018
- Import refusalRefused, Rice, plain (white or polished) processed (packaged)NO PROCESSEntry EJA-5097593-9Source
2017
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2011
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Refusal charges, in plain English
- NO PROCESS4 refused lines
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
Questions about Otoki Corporation Daepoong Factory
- Is Otoki Corporation Daepoong Factory on an FDA import alert?
- No listing for Otoki Corporation Daepoong Factory appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Korea page.
- Has FDA refused shipments from Otoki Corporation Daepoong Factory?
- Yes. FDA refused 4 shipment lines from Otoki Corporation Daepoong Factory between July 10, 2018 and August 28, 2019. The most recent, on August 28, 2019, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as NO PROCESS (no scheduled process filed).
- Why did FDA refuse Otoki Corporation Daepoong Factory's shipments?
- The most frequent charge is NO PROCESS (no scheduled process filed, 4 lines).
- When was Otoki Corporation Daepoong Factory last inspected by FDA?
- FDA's most recent inspection of Otoki Corporation Daepoong Factory with a final classification is dated September 18, 2017 and was classified VAI (Voluntary Action Indicated).
- What is Otoki Corporation Daepoong Factory's FEI number?
- Otoki Corporation Daepoong Factory's FDA Establishment Identifier (FEI) is 3009934446.
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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.