Promotora Inv Mundial SAPI de CV
FDA import alert and refusal historyRomita, MexicoFEI 3013835258
Recorded by FDA as PROMOTORA INV MUNDIAL SAPI DE CV
As of October 26, 2026, Promotora Inv Mundial SAPI de CV is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines on November 2, 2017, 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
- Pepper, hot, dried or paste · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Promotora Inv Mundial SAPI de CV
4 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalSource
Refused, 4 lines in one entry: Pepper, hot, dried or pasteFILTHYEntry BXD-0005948-4Show 4 linesHide lines
Refusal charges, in plain English
- FILTHY4 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.
Questions about Promotora Inv Mundial SAPI de CV
- Is Promotora Inv Mundial SAPI de CV on an FDA import alert?
- No listing for Promotora Inv Mundial SAPI de CV 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 Promotora Inv Mundial SAPI de CV?
- Yes. FDA refused 4 shipment lines from Promotora Inv Mundial SAPI de CV on November 2, 2017. The most recent, on November 2, 2017, was pepper, hot, dried or paste, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Promotora Inv Mundial SAPI de CV's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 4 lines).
- What is Promotora Inv Mundial SAPI de CV's FEI number?
- Promotora Inv Mundial SAPI de CV's FDA Establishment Identifier (FEI) is 3013835258.
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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.