Lanketin
FDA import alert and refusal historyGuatemala City, GuatemalaFEI 3038897849
Recorded by FDA as LANKETIN
As of October 26, 2026, Lanketin is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between August 22, 2025 and September 24, 2025, 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 Lanketin
3 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 799-1074891-4Source
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 799-1075638-8Source
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 799-0895227-0Source
Refusal charges, in plain English
- UNAPPROVED3 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 Lanketin
- Is Lanketin on an FDA import alert?
- No listing for Lanketin appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Guatemala page.
- Has FDA refused shipments from Lanketin?
- Yes. FDA refused 3 shipment lines from Lanketin between August 22, 2025 and September 24, 2025. The most recent, on September 24, 2025, 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 Lanketin's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 3 lines).
- What is Lanketin's FEI number?
- Lanketin's FDA Establishment Identifier (FEI) is 3038897849.
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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.