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Arman Ghostar Shargh Company Ltd

FDA import alert and refusal historyHerat, AfghanistanFEI 3011921272

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Example subjectArman Ghostar Shargh Company Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Arman Ghostar Shargh Company Ltd (Herat, Afghanistan) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for raisins, published by FDA on December 24, 2015, 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 Arman Ghostar Shargh Company Ltd

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

2015

  1. Import alert listing
    Listed on Import Alert 99-08red listRaisins
    Source

Questions about Arman Ghostar Shargh Company Ltd

Is Arman Ghostar Shargh Company Ltd on an FDA import alert?
Yes. As of October 26, 2026, Arman Ghostar Shargh Company Ltd is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for raisins; FDA published the listing on December 24, 2015.
Has FDA refused shipments from Arman Ghostar Shargh Company Ltd?
No FDA import refusals for Arman Ghostar Shargh Company Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Arman Ghostar Shargh Company Ltd's FEI number?
Arman Ghostar Shargh Company Ltd's FDA Establishment Identifier (FEI) is 3011921272.
Can shipments from Arman Ghostar Shargh Company Ltd still enter the U.S.?
Shipments of raisins from Arman Ghostar Shargh Company Ltd can be detained without physical examination under Import Alert 99-08; 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 subjectArman Ghostar Shargh Company Lt 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.