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Paranhae Co., Ltd

FDA import alert and refusal historySongpa, South KoreaFEI 2000038507

Recorded by FDA as PARANHAE CO., LTD

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Example subjectParanhae Co., Lt added to Import Alert 16-129 (red list)

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As of October 25, 2026, Paranhae Co., Ltd (Songpa, South Korea) is on the red list of FDA Import Alert 16-74 (Uneviscerated salt-cured, dried, smoked or fermented fish) for uneviscerated anchovy, published by FDA on May 18, 2018, and has 24 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Anchovy · MFR INSAN
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Paranhae Co., Ltd

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

2019

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2018

  1. Import refusal
    Refused, 2 lines in one entry: AnchovyMFR INSANEntry E7T-1228177-7Show 2 lines
    Source
  2. Import refusal
    Refused, AnchovyMFR INSANEntry E7T-0207186-5
    Source
  3. Import refusal
    Refused, 4 lines in one entry: AnchovyMFR INSANEntry E7T-1228177-7Show 4 lines
    Source
  4. Import refusal
    Refused, AnchovyMFR INSANEntry E7T-0207186-5
    Source
  5. Import refusal
    Refused, AnchovyMFR INSANEntry E7T-1228177-7
    Source
  6. Import refusal
    Refused, AnchovyMFR INSANEntry E7T-0207186-5
    Source
  7. Import refusal
    Refused, 4 lines in one entry: AnchovyMFR INSANEntry E7T-1228177-7Show 4 lines
    Source
  8. Import refusal
    Refused, AnchovyMFR INSANEntry E7T-0207186-5
    Source
  9. Import refusal
    Refused, AnchovyMFR INSANEntry E7T-1228177-7
    Source
  10. Import refusal
    Refused, 2 lines in one entry: AnchovyMFR INSANEntry E7T-0207186-5Show 2 lines
    Source
  11. Import refusal
    Refused, 2 lines in one entry: AnchovyMFR INSANEntry E7T-1228177-7Show 2 lines
    Source
  12. Import refusal
    Refused, AnchovyMFR INSANEntry E7T-0207186-5
    Source
  13. Import refusal
    Refused, 3 lines in one entry: AnchovyMFR INSANEntry E7T-0125188-0Show 3 lines
    Source
  14. Import alert listing
    Listed on Import Alert 16-74red listUneviscerated Anchovy
    Source

Refusal charges, in plain English

  • MFR INSAN24 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 Paranhae Co., Ltd

Is Paranhae Co., Ltd on an FDA import alert?
Yes. As of October 25, 2026, Paranhae Co., Ltd is on the red list of FDA Import Alert 16-74, “Uneviscerated salt-cured, dried, smoked or fermented fish”, for uneviscerated anchovy; FDA published the listing on May 18, 2018.
Has FDA refused shipments from Paranhae Co., Ltd?
Yes. FDA refused 24 shipment lines from Paranhae Co., Ltd between June 28, 2018 and July 2, 2018. The most recent, on July 2, 2018, was anchovy, charged as MFR INSAN (insanitary manufacturing, processing or packing).
Why did FDA refuse Paranhae Co., Ltd's shipments?
The most frequent charge is MFR INSAN (insanitary manufacturing, processing or packing, 24 lines).
When was Paranhae Co., Ltd last inspected by FDA?
FDA's most recent inspection of Paranhae Co., Ltd with a final classification is dated August 29, 2019 and was classified NAI (No Action Indicated).
What is Paranhae Co., Ltd's FEI number?
Paranhae Co., Ltd's FDA Establishment Identifier (FEI) is 2000038507.
Can shipments from Paranhae Co., Ltd still enter the U.S.?
Shipments of uneviscerated anchovy from Paranhae Co., Ltd can be detained without physical examination under Import Alert 16-74; 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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Example subjectParanhae Co., Lt added to Import Alert 16-129 (red list)

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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.