PT. Andalan Nelayan Indonesia
FDA import alert and refusal historyBogor, IndonesiaFEI 3027407862
Recorded by FDA as PT. ANDALAN NELAYAN INDONESIA
As of October 26, 2026, PT. Andalan Nelayan Indonesia is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between April 9, 2025 and March 12, 2026, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Cobia · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for PT. Andalan Nelayan Indonesia
6 records, newest first. Each line links to the FDA page it came from.
2026
2025
Refusal charges, in plain English
- FILTHY6 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about PT. Andalan Nelayan Indonesia
- Is PT. Andalan Nelayan Indonesia on an FDA import alert?
- No listing for PT. Andalan Nelayan Indonesia 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 PT. Andalan Nelayan Indonesia?
- Yes. FDA refused 6 shipment lines from PT. Andalan Nelayan Indonesia between April 9, 2025 and March 12, 2026. The most recent, on March 12, 2026, was cobia, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse PT. Andalan Nelayan Indonesia's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 6 lines).
- What is PT. Andalan Nelayan Indonesia's FEI number?
- PT. Andalan Nelayan Indonesia's FDA Establishment Identifier (FEI) is 3027407862.
Buying from PT. Andalan Nelayan Indonesia?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.