Fg Asgromex S. de R.L. de C.V.
FDA import alert and refusal historySan Miguel De Allende, MexicoFEI 3010728746
Recorded by FDA as FG ASGROMEX S. DE R.L. DE C.V.
As of October 26, 2026, Fg Asgromex S. de R.L. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between May 16, 2017 and March 10, 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
- Celery (leaf & stem vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Fg Asgromex S. de R.L. de C.V.
4 records, newest first. Each line links to the FDA page it came from.
2022
2017
Refusal charges, in plain English
- PESTICIDE4 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 Fg Asgromex S. de R.L. de C.V.
- Is Fg Asgromex S. de R.L. de C.V. on an FDA import alert?
- No listing for Fg Asgromex S. de R.L. de C.V. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
- Has FDA refused shipments from Fg Asgromex S. de R.L. de C.V.?
- Yes. FDA refused 4 shipment lines from Fg Asgromex S. de R.L. de C.V. between May 16, 2017 and March 10, 2022. The most recent, on March 10, 2022, was celery (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Fg Asgromex S. de R.L. de C.V.'s shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 4 lines).
- What is Fg Asgromex S. de R.L. de C.V.'s FEI number?
- Fg Asgromex S. de R.L. de C.V.'s FDA Establishment Identifier (FEI) is 3010728746.
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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.