Nongshim Asan Factory
FDA import alert and refusal historyAsan, South KoreaFEI 3009923971
Recorded by FDA as NONGSHIM ASAN FACTORY
As of October 26, 2026, Nongshim Asan Factory (Asan, South Korea) is on the red list of FDA Import Alert 99-31 (Food products: melamine and melamine analogs) for korean noodle soup (hooroorook), published by FDA on September 16, 2009, 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 99-31 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Nongshim Asan Factory
2 records, newest first. Each line links to the FDA page it came from.
2016
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 99-31red listKorean Noodle Soup (Hooroorook)Source
Questions about Nongshim Asan Factory
- Is Nongshim Asan Factory on an FDA import alert?
- Yes. As of October 26, 2026, Nongshim Asan Factory is on the red list of FDA Import Alert 99-31, “Food products: melamine and melamine analogs”, for korean noodle soup (hooroorook); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Nongshim Asan Factory?
- No FDA import refusals for Nongshim Asan Factory appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Nongshim Asan Factory last inspected by FDA?
- FDA's most recent inspection of Nongshim Asan Factory with a final classification is dated May 19, 2016 and was classified NAI (No Action Indicated).
- What is Nongshim Asan Factory's FEI number?
- Nongshim Asan Factory's FDA Establishment Identifier (FEI) is 3009923971.
- Can shipments from Nongshim Asan Factory still enter the U.S.?
- Shipments of korean noodle soup (hooroorook) from Nongshim Asan Factory can be detained without physical examination under Import Alert 99-31; 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.