PT Prima Rizki Perkasa
FDA import alert and refusal historyJakarta, IndonesiaFEI 2000022102
As of October 26, 2026, PT Prima Rizki Perkasa (Jakarta, Indonesia) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for tuna (albacore, yellowfin, bluefin, skipjack, etc.), published by FDA on September 18, 2009, 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 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for PT Prima Rizki Perkasa
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-81red listTuna (Albacore, Yellowfin, Bluefin, Skipjack, Etc.)Source
Questions about PT Prima Rizki Perkasa
- Is PT Prima Rizki Perkasa on an FDA import alert?
- Yes. As of October 26, 2026, PT Prima Rizki Perkasa is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for tuna (albacore, yellowfin, bluefin, skipjack, etc.); FDA published the listing on September 18, 2009.
- Has FDA refused shipments from PT Prima Rizki Perkasa?
- No FDA import refusals for PT Prima Rizki Perkasa appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is PT Prima Rizki Perkasa's FEI number?
- PT Prima Rizki Perkasa's FDA Establishment Identifier (FEI) is 2000022102.
- Can shipments from PT Prima Rizki Perkasa still enter the U.S.?
- Shipments of tuna (albacore, yellowfin, bluefin, skipjack, etc.) from PT Prima Rizki Perkasa can be detained without physical examination under Import Alert 16-81; 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).
Buying from PT Prima Rizki Perkasa?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.