PT. Awindo
FDA import alert and refusal historyJakarta Utara, IndonesiaFEI 3011249156
As of October 26, 2026, PT. Awindo is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines between August 3, 2018 and September 9, 2022, most often for histamine (HISTAMINE).
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.) · HISTAMINE
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for PT. Awindo
8 records, newest first. Each line links to the FDA page it came from.
2022
- Import refusalSource
Refused, 3 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry ES6-7004952-8Show 3 linesHide lines
2021
- Import refusalSource
Refused, 3 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry D97-1301846-0Show 3 linesHide lines
2018
Refusal charges, in plain English
- HISTAMINE6 refused lines
Histamine
The product appeared to contain histamine in a quantity that ordinarily makes it injurious to health.
- FILTHY1 refused line
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. Awindo
- Is PT. Awindo on an FDA import alert?
- No listing for PT. Awindo 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. Awindo?
- Yes. FDA refused 7 shipment lines from PT. Awindo between August 3, 2018 and September 9, 2022. The most recent, on September 9, 2022, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as HISTAMINE (histamine).
- Why did FDA refuse PT. Awindo's shipments?
- The most frequent charges are HISTAMINE (histamine, 6 lines) and FILTHY (filthy, putrid or decomposed substance, 1 line).
- When was PT. Awindo last inspected by FDA?
- FDA's most recent inspection of PT. Awindo with a final classification is dated August 3, 2018 and was classified VAI (Voluntary Action Indicated).
- What is PT. Awindo's FEI number?
- PT. Awindo's FDA Establishment Identifier (FEI) is 3011249156.
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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.