Nongshim Anyang Factory

2 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• NO PROCESS1 refused line

  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 Nongshim Anyang Factory

Is Nongshim Anyang Factory on an FDA import alert?

No listing for Nongshim Anyang 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 Nongshim Anyang Factory?

Yes. FDA refused 1 shipment line from Nongshim Anyang Factory on March 22, 2019. The most recent, on March 22, 2019, was oriental noodles (flavored with shrimp,chicken,beef,lobster,crab,plain,etc.), charged as NO PROCESS (no scheduled process filed).

Why did FDA refuse Nongshim Anyang Factory's shipments?

The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).

When was Nongshim Anyang Factory last inspected by FDA?

FDA's most recent inspection of Nongshim Anyang Factory with a final classification is dated June 2, 2016 and was classified NAI (No Action Indicated).

What is Nongshim Anyang Factory's FEI number?

Nongshim Anyang Factory's FDA Establishment Identifier (FEI) is 3011384759.