PT. Unimitra Andalan Sejati
FDA import alert and refusal historyBekasi, IndonesiaFEI 3017705684
As of October 26, 2026, PT. Unimitra Andalan Sejati is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on March 8, 2022, 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
- Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for PT. Unimitra Andalan Sejati
4 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY3 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. Unimitra Andalan Sejati
- Is PT. Unimitra Andalan Sejati on an FDA import alert?
- No listing for PT. Unimitra Andalan Sejati 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. Unimitra Andalan Sejati?
- Yes. FDA refused 3 shipment lines from PT. Unimitra Andalan Sejati on March 8, 2022. The most recent, on March 8, 2022, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse PT. Unimitra Andalan Sejati's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 3 lines).
- When was PT. Unimitra Andalan Sejati last inspected by FDA?
- FDA's most recent inspection of PT. Unimitra Andalan Sejati with a final classification is dated June 13, 2023 and was classified NAI (No Action Indicated).
- What is PT. Unimitra Andalan Sejati's FEI number?
- PT. Unimitra Andalan Sejati's FDA Establishment Identifier (FEI) is 3017705684.
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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.