PT. Lautan Niaga Jaya
FDA import alert and refusal historyJakarta, IndonesiaFEI 3004255218
As of October 26, 2026, PT. Lautan Niaga Jaya (Jakarta, Indonesia) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for frozen tuna, published by FDA on February 10, 2016, is also listed on Import Alert 16-81 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-105 · red listIA 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for PT. Lautan Niaga Jaya
2 records, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 16-105red listFrozen TunaSource
2015
- Import alert listingListed on Import Alert 16-81red listFrozen TunaSource
Questions about PT. Lautan Niaga Jaya
- Is PT. Lautan Niaga Jaya on an FDA import alert?
- Yes. As of October 26, 2026, PT. Lautan Niaga Jaya is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for frozen tuna; FDA published the listing on February 10, 2016.
- Has FDA refused shipments from PT. Lautan Niaga Jaya?
- No FDA import refusals for PT. Lautan Niaga Jaya appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is PT. Lautan Niaga Jaya's FEI number?
- PT. Lautan Niaga Jaya's FDA Establishment Identifier (FEI) is 3004255218.
- Can shipments from PT. Lautan Niaga Jaya still enter the U.S.?
- Shipments of frozen tuna from PT. Lautan Niaga Jaya can be detained without physical examination under Import Alert 16-105; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
Buying from PT. Lautan Niaga Jaya?
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.