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Arpi Mineral Water Plant JSC

FDA import alert and refusal historyVaik, ArmeniaFEI 3004328027

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Example subjectArpi Mineral Water Plant JS added to Import Alert 16-129 (red list)

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As of October 26, 2026, Arpi Mineral Water Plant JSC (Vaik, Armenia) is on the red list of FDA Import Alert 99-42 (Foods: heavy metal (toxic element) contamination) for bottled water, published by FDA on March 3, 2022, 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 Arpi Mineral Water Plant JSC

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

2022

  1. Import alert listing
    Listed on Import Alert 99-42red listBottled Water
    Source

Questions about Arpi Mineral Water Plant JSC

Is Arpi Mineral Water Plant JSC on an FDA import alert?
Yes. As of October 26, 2026, Arpi Mineral Water Plant JSC is on the red list of FDA Import Alert 99-42, “Foods: heavy metal (toxic element) contamination”, for bottled water; FDA published the listing on March 3, 2022.
Has FDA refused shipments from Arpi Mineral Water Plant JSC?
No FDA import refusals for Arpi Mineral Water Plant JSC appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Arpi Mineral Water Plant JSC's FEI number?
Arpi Mineral Water Plant JSC's FDA Establishment Identifier (FEI) is 3004328027.
Can shipments from Arpi Mineral Water Plant JSC still enter the U.S.?
Shipments of bottled water from Arpi Mineral Water Plant JSC can be detained without physical examination under Import Alert 99-42; 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 subjectArpi Mineral Water Plant JS 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.