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Fpc Group, S.A.

FDA import alert and refusal historyCiudad Vieja, GuatemalaFEI 3011896976

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Example subjectFpc Group, S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Fpc Group, S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on April 8, 2026, most often for pesticide chemical residue (PESTICIDE).

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

Current status

Import alerts
Not listed
Last import refusal
Pineapple (subtropical and tropical fruit) · PESTICIDE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Fpc Group, S.A.

1 record, newest first. Each line links to the FDA page it came from.

2026

  1. Import refusal
    Refused, Pineapple (subtropical and tropical fruit)PESTICIDEEntry NX2-0055438-4
    Source

Refusal charges, in plain English

  • PESTICIDE1 refused line

    Pesticide chemical residue

    The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

Questions about Fpc Group, S.A.

Is Fpc Group, S.A. on an FDA import alert?
No listing for Fpc Group, 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 Guatemala page.
Has FDA refused shipments from Fpc Group, S.A.?
Yes. FDA refused 1 shipment line from Fpc Group, S.A. on April 8, 2026. The most recent, on April 8, 2026, was pineapple (subtropical and tropical fruit), charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse Fpc Group, S.A.'s shipments?
The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
What is Fpc Group, S.A.'s FEI number?
Fpc Group, S.A.'s FDA Establishment Identifier (FEI) is 3011896976.

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Example subjectFpc Group, 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.