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PT. Patroman Senoputra

FDA import alert and refusal historyBandarlampung, IndonesiaFEI 3004280201

Recorded by FDA as PT. PATROMAN SENOPUTRA

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Example subjectPT. Patroman Senoputr added to Import Alert 16-129 (red list)

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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

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

  1. Import alert listing
    Listed on Import Alert 99-19red listWhole Black Pepper
    Source

2016

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

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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Example subjectPT. Patroman Senoputr added to Import Alert 16-129 (red list)

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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.