Proimec S.A.
FDA import alert and refusal historyManta, EcuadorFEI 3006310249
Recorded by FDA as PROIMEC S.A.
As of October 26, 2026, Proimec S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 5 of its shipment lines between February 22, 2023 and May 2, 2023, 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 · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Proimec S.A.
6 records, newest first. Each line links to the FDA page it came from.
2023
2018
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
Refusal charges, in plain English
- FILTHY5 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.
- HISTAMINE1 refused line
Histamine
The product appeared to contain histamine in a quantity that ordinarily makes it injurious to health.
Questions about Proimec S.A.
- Is Proimec S.A. on an FDA import alert?
- No listing for Proimec S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Ecuador page.
- Has FDA refused shipments from Proimec S.A.?
- Yes. FDA refused 5 shipment lines from Proimec S.A. between February 22, 2023 and May 2, 2023. The most recent, on May 2, 2023, was mahi mahi, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Proimec S.A.'s shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 5 lines) and HISTAMINE (histamine, 1 line).
- When was Proimec S.A. last inspected by FDA?
- FDA's most recent inspection of Proimec S.A. with a final classification is dated July 17, 2018 and was classified NAI (No Action Indicated).
- What is Proimec S.A.'s FEI number?
- Proimec S.A.'s FDA Establishment Identifier (FEI) is 3006310249.
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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.