PT. Windika Utama
FDA import alert and refusal historySemarang, IndonesiaFEI 3000255965
As of October 26, 2026, PT. Windika Utama (Semarang, Indonesia) is on the red list of FDA Import Alert 16-127 (Seafood: chloramphenicol) for crabmeat, published by FDA on August 14, 2010, 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 16-127 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for PT. Windika Utama
2 records, newest first. Each line links to the FDA page it came from.
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2010
- Import alert listingListed on Import Alert 16-127red listCrabmeatSource
Questions about PT. Windika Utama
- Is PT. Windika Utama on an FDA import alert?
- Yes. As of October 26, 2026, PT. Windika Utama is on the red list of FDA Import Alert 16-127, “Seafood: chloramphenicol”, for crabmeat; FDA published the listing on August 14, 2010.
- Has FDA refused shipments from PT. Windika Utama?
- No FDA import refusals for PT. Windika Utama appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was PT. Windika Utama last inspected by FDA?
- FDA's most recent inspection of PT. Windika Utama with a final classification is dated March 23, 2012 and was classified VAI (Voluntary Action Indicated).
- What is PT. Windika Utama's FEI number?
- PT. Windika Utama's FDA Establishment Identifier (FEI) is 3000255965.
- Can shipments from PT. Windika Utama still enter the U.S.?
- Shipments of crabmeat from PT. Windika Utama can be detained without physical examination under Import Alert 16-127; 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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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.