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Industrial Pesquera Santa Priscila S.A. (Factory 2)

FDA import alert and refusal historyGuayaquil, EcuadorFEI 3010798999

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Example subjectIndustrial Pesquera Santa Priscila S.A. (Factory 2 added to Import Alert 16-129 (red list)

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As of October 27, 2026, Industrial Pesquera Santa Priscila S.A. (Factory 2) is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines between May 27, 2022 and June 16, 2026, most often for salmonella (SALMONELLA).

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

Current status

Import alerts
Not listed
Last import refusal
Shrimp and prawns, aquaculture harvested fishery/seafood products · SALMONELLA
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Industrial Pesquera Santa Priscila S.A. (Factory 2)

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

2026

  1. Import refusal
    Refused, 2 lines in one entry: Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 594-0410443-8Show 2 lines
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 594-0410443-8Source
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 594-0410443-8Source
    Source

2022

  1. Import refusal
    Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 082-0431695-7
    Source
  2. Import refusal
    Refused, 3 lines in one entry: Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 224-4631282-3Show 3 lines
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 224-4631282-3Source
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 224-4631282-3Source
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 224-4631282-3Source
    Source
  3. Import refusal
    Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry AQZ-0535050-2
    Source

2019

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

2014

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

Refusal charges, in plain English

  • SALMONELLA7 refused lines

    Salmonella

    The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

Questions about Industrial Pesquera Santa Priscila S.A. (Factory 2)

Is Industrial Pesquera Santa Priscila S.A. (Factory 2) on an FDA import alert?
No listing for Industrial Pesquera Santa Priscila S.A. (Factory 2) appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Ecuador page.
Has FDA refused shipments from Industrial Pesquera Santa Priscila S.A. (Factory 2)?
Yes. FDA refused 7 shipment lines from Industrial Pesquera Santa Priscila S.A. (Factory 2) between May 27, 2022 and June 16, 2026. The most recent, on June 16, 2026, was shrimp and prawns, aquaculture harvested fishery/seafood products, charged as SALMONELLA (salmonella).
Why did FDA refuse Industrial Pesquera Santa Priscila S.A. (Factory 2)'s shipments?
The most frequent charge is SALMONELLA (salmonella, 7 lines).
When was Industrial Pesquera Santa Priscila S.A. (Factory 2) last inspected by FDA?
FDA's most recent inspection of Industrial Pesquera Santa Priscila S.A. (Factory 2) with a final classification is dated June 6, 2019 and was classified VAI (Voluntary Action Indicated).
What is Industrial Pesquera Santa Priscila S.A. (Factory 2)'s FEI number?
Industrial Pesquera Santa Priscila S.A. (Factory 2)'s FDA Establishment Identifier (FEI) is 3010798999.

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Example subjectIndustrial Pesquera Santa Priscila S.A. (Factory 2 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.