Urufarma
FDA import alert and refusal historyMontevideo, UruguayFEI 3013042026
Recorded by FDA as URUFARMA
As of October 25, 2026, Urufarma is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on August 21, 2017, most often for required label information not in english (NO ENGLISH).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin b12 (cyanocobalamin) · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Urufarma
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalSource
Refused, 2 lines in one entry: Vitamin b12 (cyanocobalamin); Potassium (mineral)NO ENGLISHUNAPPROVEDEntry 799-1756786-6Show 2 linesHide lines
- Refused, Vitamin b12 (cyanocobalamin)NO ENGLISHUNAPPROVEDEntry 799-1756786-6Source
- Refused, Potassium (mineral)NO ENGLISHUNAPPROVEDEntry 799-1756786-6Source
Refusal charges, in plain English
- NO ENGLISH2 refused lines
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
- UNAPPROVED2 refused lines
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.
Questions about Urufarma
- Is Urufarma on an FDA import alert?
- No listing for Urufarma appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Uruguay page.
- Has FDA refused shipments from Urufarma?
- Yes. FDA refused 2 shipment lines from Urufarma on August 21, 2017. The most recent, on August 21, 2017, was vitamin b12 (cyanocobalamin), charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Urufarma's shipments?
- The most frequent charges are NO ENGLISH (required label information not in english, 2 lines) and UNAPPROVED (unapproved new drug, 2 lines).
- What is Urufarma's FEI number?
- Urufarma's FDA Establishment Identifier (FEI) is 3013042026.
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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.