Pacfish S.A.
FDA import alert and refusal historyGuayaquil, EcuadorFEI 3006232869
As of October 25, 2026, Pacfish S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 10, 2016, 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
- Mahi mahi · HISTAMINE
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Pacfish S.A.
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY1 refused line
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.
- HISTAMINE1 refused line
Histamine
The product appeared to contain histamine in a quantity that ordinarily makes it injurious to health.
Questions about Pacfish S.A.
- Is Pacfish S.A. on an FDA import alert?
- No listing for Pacfish 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 Ecuador page.
- Has FDA refused shipments from Pacfish S.A.?
- Yes. FDA refused 1 shipment line from Pacfish S.A. on November 10, 2016. The most recent, on November 10, 2016, was mahi mahi, charged as HISTAMINE (histamine).
- Why did FDA refuse Pacfish S.A.'s shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 1 line) and HISTAMINE (histamine, 1 line).
- When was Pacfish S.A. last inspected by FDA?
- FDA's most recent inspection of Pacfish S.A. with a final classification is dated April 16, 2013 and was classified VAI (Voluntary Action Indicated).
- What is Pacfish S.A.'s FEI number?
- Pacfish S.A.'s FDA Establishment Identifier (FEI) is 3006232869.
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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.