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Pt. Hakiwa Mandiri Putra

FDA import alert and refusal historyBandarlampung, IndonesiaFEI 3002838543

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Example subjectPt. Hakiwa Mandiri Putr added to Import Alert 16-129 (red list)

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As of October 26, 2026, Pt. Hakiwa Mandiri Putra (Bandarlampung, Indonesia) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for pepper, black, ground, cracked (spice), published by FDA on September 16, 2009, 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
None on record

Every FDA record for Pt. Hakiwa Mandiri Putra

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 99-19red listPepper, Black, Ground, Cracked (Spice)
    Source

Questions about Pt. Hakiwa Mandiri Putra

Is Pt. Hakiwa Mandiri Putra on an FDA import alert?
Yes. As of October 26, 2026, Pt. Hakiwa Mandiri Putra is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for pepper, black, ground, cracked (spice); FDA published the listing on September 16, 2009.
Has FDA refused shipments from Pt. Hakiwa Mandiri Putra?
No FDA import refusals for Pt. Hakiwa Mandiri Putra appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Pt. Hakiwa Mandiri Putra's FEI number?
Pt. Hakiwa Mandiri Putra's FDA Establishment Identifier (FEI) is 3002838543.
Can shipments from Pt. Hakiwa Mandiri Putra still enter the U.S.?
Shipments of pepper, black, ground, cracked (spice) from Pt. Hakiwa Mandiri Putra 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. Hakiwa Mandiri Putr 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.