PT Awindo International
FDA import alert and refusal historyJakarta, IndonesiaFEI 3007584623
As of October 26, 2026, PT Awindo International (Jakarta, Indonesia) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for tuna, published by FDA on July 30, 2013, 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
- Classified NAI (No Action Indicated)
Every FDA record for PT Awindo International
3 records, newest first. Each line links to the FDA page it came from.
2018
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2013
- Import alert listingListed on Import Alert 16-105red listTunaSource
- Import alert listingListed on Import Alert 16-81red listTunaSource
Questions about PT Awindo International
- Is PT Awindo International on an FDA import alert?
- Yes. As of October 26, 2026, PT Awindo International is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for tuna; FDA published the listing on July 30, 2013.
- Has FDA refused shipments from PT Awindo International?
- No FDA import refusals for PT Awindo International appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was PT Awindo International last inspected by FDA?
- FDA's most recent inspection of PT Awindo International with a final classification is dated July 3, 2018 and was classified NAI (No Action Indicated).
- What is PT Awindo International's FEI number?
- PT Awindo International's FDA Establishment Identifier (FEI) is 3007584623.
- Can shipments from PT Awindo International still enter the U.S.?
- Shipments of tuna from PT Awindo International 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).
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