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Michelle Gleneuine

FDA import alert and refusal historyRio de Janeiro, BrazilFEI 3005524067

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Example subjectMichelle Gleneuin added to Import Alert 16-129 (red list)

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As of October 26, 2026, Michelle Gleneuine (Rio de Janeiro, Brazil) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for peb one and peb two capsules (brand renutryent) dietary supplement, published by FDA on May 11, 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 Michelle Gleneuine

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

2015

  1. Import alert listing
    Listed on Import Alert 54-16red listPEB One and PEB Two Capsules (Brand Renutryent) Dietary Supplement
    Source

Questions about Michelle Gleneuine

Is Michelle Gleneuine on an FDA import alert?
Yes. As of October 26, 2026, Michelle Gleneuine is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for peb one and peb two capsules (brand renutryent) dietary supplement; FDA published the listing on May 11, 2015.
Has FDA refused shipments from Michelle Gleneuine?
No FDA import refusals for Michelle Gleneuine appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Michelle Gleneuine's FEI number?
Michelle Gleneuine's FDA Establishment Identifier (FEI) is 3005524067.
Can shipments from Michelle Gleneuine still enter the U.S.?
Shipments of peb one and peb two capsules (brand renutryent) dietary supplement from Michelle Gleneuine can be detained without physical examination under Import Alert 54-16; 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 subjectMichelle Gleneuin 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.