SupplierRadar

C.I Grupex S.A.S

FDA import alert and refusal historyBogota, ColombiaFEI 3016607158

Recorded by FDA as C.I GRUPEX S.A.S

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Example subjectC.I Grupex S.A. added to Import Alert 16-129 (red list)

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As of October 26, 2026, C.I Grupex S.A.S is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on September 16, 2022, 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
Lime (citrus) · PESTICIDE
Last warning letter
None found
Last inspection
None on record

Every FDA record for C.I Grupex S.A.S

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

2022

  1. Import refusal
    Refused, 2 lines in one entry: Lime (citrus)PESTICIDEEntry 9P3-0257420-3Show 2 lines
    Source

Refusal charges, in plain English

  • PESTICIDE2 refused lines

    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 C.I Grupex S.A.S

Is C.I Grupex S.A.S on an FDA import alert?
No listing for C.I Grupex S.A.S appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Colombia page.
Has FDA refused shipments from C.I Grupex S.A.S?
Yes. FDA refused 2 shipment lines from C.I Grupex S.A.S on September 16, 2022. The most recent, on September 16, 2022, was lime (citrus), charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse C.I Grupex S.A.S's shipments?
The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
What is C.I Grupex S.A.S's FEI number?
C.I Grupex S.A.S's FDA Establishment Identifier (FEI) is 3016607158.

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Example subjectC.I Grupex 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.