PT. Tonga Tiur Putra
FDA import alert and refusal historyRembang, IndonesiaFEI 3004250032
As of October 25, 2026, PT. Tonga Tiur Putra (Rembang, Indonesia) is on the red list of FDA Import Alert 16-127 (Seafood: chloramphenicol) for crabmeat, published by FDA on October 1, 2009, 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 16-127 · red listIA 16-81 · 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. Tonga Tiur Putra
3 records, newest first. Each line links to the FDA page it came from.
2011
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 16-127red listCrabmeatSource
- Import alert listingListed on Import Alert 16-81red listSnapper; Crab; Lobster; Spiny Lobster, Rock Lobster; Slipper LobsterSource
Questions about PT. Tonga Tiur Putra
- Is PT. Tonga Tiur Putra on an FDA import alert?
- Yes. As of October 25, 2026, PT. Tonga Tiur Putra is on the red list of FDA Import Alert 16-127, “Seafood: chloramphenicol”, for crabmeat; FDA published the listing on October 1, 2009.
- Has FDA refused shipments from PT. Tonga Tiur Putra?
- No FDA import refusals for PT. Tonga Tiur Putra appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was PT. Tonga Tiur Putra last inspected by FDA?
- FDA's most recent inspection of PT. Tonga Tiur Putra with a final classification is dated May 13, 2011 and was classified VAI (Voluntary Action Indicated).
- What is PT. Tonga Tiur Putra's FEI number?
- PT. Tonga Tiur Putra's FDA Establishment Identifier (FEI) is 3004250032.
- Can shipments from PT. Tonga Tiur Putra still enter the U.S.?
- Shipments of crabmeat from PT. Tonga Tiur Putra 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.