Machoen Nonghyup
FDA import alert and refusal historyHamyang-gun, South KoreaFEI 3006618180
As of October 26, 2026, Machoen Nonghyup (Hamyang-gun, South Korea) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for dried taro root; dried potato stem; dried radish (nongbuga), published by FDA on October 14, 2011, 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 99-08 · 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 Machoen Nonghyup
2 records, newest first. Each line links to the FDA page it came from.
2017
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2011
- Import alert listingListed on Import Alert 99-08red listDried Taro Root; Dried Potato Stem; Dried Radish (Nongbuga)Source
Questions about Machoen Nonghyup
- Is Machoen Nonghyup on an FDA import alert?
- Yes. As of October 26, 2026, Machoen Nonghyup is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for dried taro root; dried potato stem; dried radish (nongbuga); FDA published the listing on October 14, 2011.
- Has FDA refused shipments from Machoen Nonghyup?
- No FDA import refusals for Machoen Nonghyup appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Machoen Nonghyup last inspected by FDA?
- FDA's most recent inspection of Machoen Nonghyup with a final classification is dated March 28, 2017 and was classified NAI (No Action Indicated).
- What is Machoen Nonghyup's FEI number?
- Machoen Nonghyup's FDA Establishment Identifier (FEI) is 3006618180.
- Can shipments from Machoen Nonghyup still enter the U.S.?
- Shipments of dried taro root; dried potato stem; dried radish (nongbuga) from Machoen Nonghyup can be detained without physical examination under Import Alert 99-08; 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.