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Nicalapia S.A.

FDA import alert and refusal historyLeon, NicaraguaFEI 3003119233

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Example subjectNicalapia S.A added to Import Alert 16-129 (red list)

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As of October 25, 2026, Nicalapia S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 14 of its shipment lines between January 8, 2018 and November 1, 2024, most often for filthy, putrid or decomposed substance (FILTHY).

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

Current status

Import alerts
Not listed
Last import refusal
Spiny lobster, rock lobster · FILTHY
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Nicalapia S.A.

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

2024

  1. Import refusal
    Refused, 3 lines in one entry: Spiny lobster, rock lobsterFILTHYNO ENGLISHNUTRIT LBLEntry RC9-0033599-8Show 3 lines
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Spiny lobster, rock lobsterFILTHYEntry RC9-0033552-7Show 2 lines
    • Refused, Spiny lobster, rock lobsterFILTHYEntry RC9-0033552-7Source
    • Refused, Spiny lobster, rock lobsterFILTHYEntry RC9-0033552-7Source
    Source

2023

  1. Import refusal
    Refused, GroupersFILTHYEntry RC9-0032227-7
    Source

2022

  1. Import refusal
    Refused, GroupersFILTHYEntry RC9-0031976-0
    Source
  2. Import refusal
    Refused, Mahi mahiFILTHYEntry RC9-0031420-9
    Source

2019

  1. Import refusal
    Refused, Mahi mahiFILTHYEntry RC9-0028634-0
    Source

2018

  1. Import refusal
    Refused, Mahi mahiFILTHYEntry RC9-0027967-5
    Source
  2. Import refusal
    Refused, Mahi mahiFILTHYEntry RC9-0028050-9
    Source
  3. Import refusal
    Refused, Mahi mahiFILTHYEntry RC9-0028020-2
    Source
  4. Import refusal
    Refused, Mahi mahiFILTHYEntry RC9-0027912-1
    Source
  5. Import refusal
    Refused, Mahi mahiFILTHYEntry RC9-0027528-5
    Source

2013

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2011

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • FILTHY14 refused lines

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

  • NO ENGLISH3 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • NUTRIT LBL3 refused lines

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about Nicalapia S.A.

Is Nicalapia S.A. on an FDA import alert?
No listing for Nicalapia S.A. appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Nicaragua page.
Has FDA refused shipments from Nicalapia S.A.?
Yes. FDA refused 14 shipment lines from Nicalapia S.A. between January 8, 2018 and November 1, 2024. The most recent, on November 1, 2024, was spiny lobster, rock lobster, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Nicalapia S.A.'s shipments?
The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 14 lines) and NO ENGLISH (required label information not in english, 3 lines).
When was Nicalapia S.A. last inspected by FDA?
FDA's most recent inspection of Nicalapia S.A. with a final classification is dated August 16, 2013 and was classified VAI (Voluntary Action Indicated).
What is Nicalapia S.A.'s FEI number?
Nicalapia S.A.'s FDA Establishment Identifier (FEI) is 3003119233.

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Example subjectNicalapia S.A 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.