Raquel Urena
FDA import alert and refusal historySanto Domingo, Dominican RepublicFEI 3018688881
Recorded by FDA as RAQUEL URENA
As of October 26, 2026, Raquel Urena is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 17, 2021, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Raquel Urena
1 record, newest first. Each line links to the FDA page it came from.
2021
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry SCS-5377821-5Source
Refusal charges, in plain English
- 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.
Questions about Raquel Urena
- Is Raquel Urena on an FDA import alert?
- No listing for Raquel Urena appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Dominican Republic page.
- Has FDA refused shipments from Raquel Urena?
- Yes. FDA refused 1 shipment line from Raquel Urena on May 17, 2021. The most recent, on May 17, 2021, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Raquel Urena's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Raquel Urena's FEI number?
- Raquel Urena's FDA Establishment Identifier (FEI) is 3018688881.
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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.