PT. Patroman Senoputra
FDA import alert and refusal historyBandarlampung, IndonesiaFEI 3004280201
Recorded by FDA as PT. PATROMAN SENOPUTRA
As of October 26, 2026, PT. Patroman Senoputra (Bandarlampung, Indonesia) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for whole black pepper, published by FDA on January 18, 2017, 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 99-19 · 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. Patroman Senoputra
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import alert listingListed on Import Alert 99-19red listWhole Black PepperSource
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about PT. Patroman Senoputra
- Is PT. Patroman Senoputra on an FDA import alert?
- Yes. As of October 26, 2026, PT. Patroman Senoputra is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for whole black pepper; FDA published the listing on January 18, 2017.
- Has FDA refused shipments from PT. Patroman Senoputra?
- No FDA import refusals for PT. Patroman Senoputra appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was PT. Patroman Senoputra last inspected by FDA?
- FDA's most recent inspection of PT. Patroman Senoputra with a final classification is dated May 31, 2016 and was classified VAI (Voluntary Action Indicated).
- What is PT. Patroman Senoputra's FEI number?
- PT. Patroman Senoputra's FDA Establishment Identifier (FEI) is 3004280201.
- Can shipments from PT. Patroman Senoputra still enter the U.S.?
- Shipments of whole black pepper from PT. Patroman Senoputra can be detained without physical examination under Import Alert 99-19; 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.