Hekim Ilac Medikal Kozmetik San
FDA import alert and refusal historyIstanbul, TurkeyFEI 3044064915
Recorded by FDA as HEKIM ILAC MEDIKAL KOZMETIK SAN
As of October 27, 2026, Hekim Ilac Medikal Kozmetik San is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 9, 2026, 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
- L-arginine (protein) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Hekim Ilac Medikal Kozmetik San
1 record, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, L-arginine (protein)UNAPPROVEDEntry AEK-0510827-8Source
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 Hekim Ilac Medikal Kozmetik San
- Is Hekim Ilac Medikal Kozmetik San on an FDA import alert?
- No listing for Hekim Ilac Medikal Kozmetik San appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Turkey page.
- Has FDA refused shipments from Hekim Ilac Medikal Kozmetik San?
- Yes. FDA refused 1 shipment line from Hekim Ilac Medikal Kozmetik San on September 9, 2026. The most recent, on September 9, 2026, was l-arginine (protein), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Hekim Ilac Medikal Kozmetik San's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Hekim Ilac Medikal Kozmetik San's FEI number?
- Hekim Ilac Medikal Kozmetik San's FDA Establishment Identifier (FEI) is 3044064915.
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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.