Immuno Venture Products Limited
FDA import alert and refusal historyMay Pen, JamaicaFEI 3008343737
As of October 26, 2026, Immuno Venture Products Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 22, 2023, 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
- Herbals & botanicals (not teas), n.e.c. · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Immuno Venture Products Limited
1 record, newest first. Each line links to the FDA page it came from.
2023
- Import refusalRefused, Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry 8YV-0001433-2Source
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 Immuno Venture Products Limited
- Is Immuno Venture Products Limited on an FDA import alert?
- No listing for Immuno Venture Products Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Jamaica page.
- Has FDA refused shipments from Immuno Venture Products Limited?
- Yes. FDA refused 1 shipment line from Immuno Venture Products Limited on June 22, 2023. The most recent, on June 22, 2023, was herbals & botanicals (not teas), n.e.c., charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Immuno Venture Products Limited's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Immuno Venture Products Limited's FEI number?
- Immuno Venture Products Limited's FDA Establishment Identifier (FEI) is 3008343737.
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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.