UD. Maju Jaya
FDA import alert and refusal historyKota Palembang, IndonesiaFEI 3015176561
As of October 26, 2026, UD. Maju Jaya is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 16, 2020, most often for fair packaging and labeling act (LABELING).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Kratom (herbal and botanicals, not teas ii) · UNSFDIETLB
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for UD. Maju Jaya
1 record, newest first. Each line links to the FDA page it came from.
2020
- Import refusalRefused, Kratom (herbal and botanicals, not teas ii)UNSFDIETLBLABELINGSALMONELLAEntry 9DH-0027720-7Source
Refusal charges, in plain English
- LABELING1 refused line
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
- UNSFDIETLB1 refused line
UNSFDIETLB
Questions about UD. Maju Jaya
- Is UD. Maju Jaya on an FDA import alert?
- No listing for UD. Maju Jaya appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Indonesia page.
- Has FDA refused shipments from UD. Maju Jaya?
- Yes. FDA refused 1 shipment line from UD. Maju Jaya on May 16, 2020. The most recent, on May 16, 2020, was kratom (herbal and botanicals, not teas ii), charged as UNSFDIETLB (unsfdietlb).
- Why did FDA refuse UD. Maju Jaya's shipments?
- The most frequent charges are LABELING (fair packaging and labeling act, 1 line) and SALMONELLA (salmonella, 1 line).
- What is UD. Maju Jaya's FEI number?
- UD. Maju Jaya's FDA Establishment Identifier (FEI) is 3015176561.
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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.