Dromeinter
FDA import alert and refusal historyTegucigalpa, HondurasFEI 3020047550
Recorded by FDA as DROMEINTER
As of October 25, 2026, Dromeinter is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between April 21, 2022 and September 19, 2022, 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
- Vitamin b12 (cyanocobalamin) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Dromeinter
2 records, newest first. Each line links to the FDA page it came from.
2022
- Import refusalRefused, Vitamin b12 (cyanocobalamin)UNAPPROVEDEntry AMN-0072276-5Source
- Import refusalRefused, Multiple vitamins (mvi-12 vitamin combo) (vitamin)LIST INGREFILTHYLACKS FIRMLACKS N/CUSUAL NAMEEntry AMN-0072927-3Source
Refusal charges, in plain English
- FILTHY1 refused line
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.
- LACKS FIRM1 refused line
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- LACKS N/C1 refused line
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- LIST INGRE1 refused line
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- UNAPPROVED1 refused line
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
- USUAL NAME1 refused line
Common or usual name missing
The label appeared not to show the common or usual name of the food.
Questions about Dromeinter
- Is Dromeinter on an FDA import alert?
- No listing for Dromeinter appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Honduras page.
- Has FDA refused shipments from Dromeinter?
- Yes. FDA refused 2 shipment lines from Dromeinter between April 21, 2022 and September 19, 2022. The most recent, on September 19, 2022, was vitamin b12 (cyanocobalamin), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Dromeinter's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 1 line) and LACKS FIRM (manufacturer name and address missing, 1 line).
- What is Dromeinter's FEI number?
- Dromeinter's FDA Establishment Identifier (FEI) is 3020047550.
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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.