Rosario Elizabeth Monterrosas Ro
FDA import alert and refusal historyPuebla, MexicoFEI 3014678567
Recorded by FDA as ROSARIO ELIZABETH MONTERROSAS RO
As of October 26, 2026, Rosario Elizabeth Monterrosas Ro is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on September 21, 2018, most often for insanitary manufacturing, processing or packing (MFR INSAN).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Cilantro (leaf & stem vegetable) · MFR INSAN
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Rosario Elizabeth Monterrosas Ro
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- MFR INSAN2 refused lines
Insanitary manufacturing, processing or packing
The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.
Questions about Rosario Elizabeth Monterrosas Ro
- Is Rosario Elizabeth Monterrosas Ro on an FDA import alert?
- No listing for Rosario Elizabeth Monterrosas Ro 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 Rosario Elizabeth Monterrosas Ro?
- Yes. FDA refused 2 shipment lines from Rosario Elizabeth Monterrosas Ro on September 21, 2018. The most recent, on September 21, 2018, was cilantro (leaf & stem vegetable), charged as MFR INSAN (insanitary manufacturing, processing or packing).
- Why did FDA refuse Rosario Elizabeth Monterrosas Ro's shipments?
- The most frequent charge is MFR INSAN (insanitary manufacturing, processing or packing, 2 lines).
- What is Rosario Elizabeth Monterrosas Ro's FEI number?
- Rosario Elizabeth Monterrosas Ro's FDA Establishment Identifier (FEI) is 3014678567.
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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.