OSUNG Fisheries
FDA import alert and refusal historyYeosu-City, South KoreaFEI 3013479706
As of October 26, 2026, OSUNG Fisheries is on the green list of FDA Import Alert 16-74, which exempts its listed products from detention without physical examination under that alert, and has 6 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-74 · green list
- Last import refusal
- Anchovy · MFR INSAN
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for OSUNG Fisheries
7 records, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 16-74green listAnchovySource
2017
Refusal charges, in plain English
- MFR INSAN6 refused lines
Insanitary manufacturing, processing or packing
The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.
Questions about OSUNG Fisheries
- Is OSUNG Fisheries on an FDA import alert?
- Yes. As of October 26, 2026, OSUNG Fisheries is on the green list of FDA Import Alert 16-74, “Uneviscerated salt-cured, dried, smoked or fermented fish”, for anchovy; FDA published the listing on December 13, 2023.
- Has FDA refused shipments from OSUNG Fisheries?
- Yes. FDA refused 6 shipment lines from OSUNG Fisheries between August 1, 2017 and August 17, 2017. The most recent, on August 17, 2017, was anchovy, charged as MFR INSAN (insanitary manufacturing, processing or packing).
- Why did FDA refuse OSUNG Fisheries's shipments?
- The most frequent charge is MFR INSAN (insanitary manufacturing, processing or packing, 6 lines).
- What is OSUNG Fisheries's FEI number?
- OSUNG Fisheries's FDA Establishment Identifier (FEI) is 3013479706.
Buying from OSUNG Fisheries?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.