SupplierRadar

Acdima International

FDA import alert and refusal historyGiza, EgyptFEI 3014742406

Recorded by FDA as ACDIMA INTERNATIONAL

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Example subjectAcdima Internationa added to Import Alert 16-129 (red list)

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As of October 26, 2026, Acdima International is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 5, 2019, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Vitamin k (phytonadione) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Acdima International

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

2019

  1. Import refusal
    Refused, Vitamin k (phytonadione)UNAPPROVEDEntry 799-0223488-7
    Source

Refusal charges, in plain English

  • UNAPPROVED1 refused line

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Acdima International

Is Acdima International on an FDA import alert?
No listing for Acdima International appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Egypt page.
Has FDA refused shipments from Acdima International?
Yes. FDA refused 1 shipment line from Acdima International on June 5, 2019. The most recent, on June 5, 2019, was vitamin k (phytonadione), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Acdima International's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Acdima International's FEI number?
Acdima International's FDA Establishment Identifier (FEI) is 3014742406.

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Example subjectAcdima Internationa 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.