Jeong Poong Co., Ltd
FDA import alert and refusal historyCheonan-si, South KoreaFEI 2000003228
As of October 26, 2026, Jeong Poong Co., Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on December 8, 2016, most often for processor not registered for canned or acidified foods (NEEDS FCE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Broth, seafood (n.e.c.), fishery products, n.e.c. · NEEDS FCE
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Jeong Poong Co., Ltd
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- NEEDS FCE2 refused lines
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
Questions about Jeong Poong Co., Ltd
- Is Jeong Poong Co., Ltd on an FDA import alert?
- No listing for Jeong Poong Co., Ltd 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 Jeong Poong Co., Ltd?
- Yes. FDA refused 2 shipment lines from Jeong Poong Co., Ltd on December 8, 2016. The most recent, on December 8, 2016, was broth, seafood (n.e.c.), fishery products, n.e.c., charged as NEEDS FCE (processor not registered for canned or acidified foods).
- Why did FDA refuse Jeong Poong Co., Ltd's shipments?
- The most frequent charge is NEEDS FCE (processor not registered for canned or acidified foods, 2 lines).
- When was Jeong Poong Co., Ltd last inspected by FDA?
- FDA's most recent inspection of Jeong Poong Co., Ltd with a final classification is dated June 2, 2016 and was classified NAI (No Action Indicated).
- What is Jeong Poong Co., Ltd's FEI number?
- Jeong Poong Co., Ltd's FDA Establishment Identifier (FEI) is 2000003228.
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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.