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CV Buana Permai

FDA import alert and refusal historyTelikbetung, IndonesiaFEI 3004336107

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Example subjectCV Buana Perma added to Import Alert 16-129 (red list)

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As of October 26, 2026, CV Buana Permai (Telikbetung, Indonesia) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for pepper,black, whole (spice); 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 CV Buana Permai

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, Whole (Spice); Pepper, Black, Ground, Cracked (Spice)
    Source

Questions about CV Buana Permai

Is CV Buana Permai on an FDA import alert?
Yes. As of October 26, 2026, CV Buana Permai is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for pepper,black, whole (spice); pepper, black, ground, cracked (spice); FDA published the listing on September 16, 2009.
Has FDA refused shipments from CV Buana Permai?
No FDA import refusals for CV Buana Permai appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is CV Buana Permai's FEI number?
CV Buana Permai's FDA Establishment Identifier (FEI) is 3004336107.
Can shipments from CV Buana Permai still enter the U.S.?
Shipments of pepper,black, whole (spice); pepper, black, ground, cracked (spice) from CV Buana Permai 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 subjectCV Buana Perma 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.