Vemedia
FDA import alert and refusal historyLondon, United KingdomFEI 3015341006
Recorded by FDA as VEMEDIA
As of October 25, 2026, Vemedia is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on June 3, 2019, most often for required label information not in english (NO ENGLISH).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin c (ascorbic acid) · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Vemedia
3 records, newest first. Each line links to the FDA page it came from.
2019
- Import refusalSource
Refused, 3 lines in one entry: Vitamin c (ascorbic acid)NO ENGLISHEntry SCS-4781192-3Show 3 linesHide lines
- Refused, Vitamin c (ascorbic acid)NO ENGLISHEntry SCS-4781192-3Source
- Refused, Vitamin c (ascorbic acid)NO ENGLISHEntry SCS-4781192-3Source
- Refused, Vitamin c (ascorbic acid)NO ENGLISHEntry SCS-4781192-3Source
Refusal charges, in plain English
- NO ENGLISH3 refused lines
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
Questions about Vemedia
- Is Vemedia on an FDA import alert?
- No listing for Vemedia appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the United Kingdom page.
- Has FDA refused shipments from Vemedia?
- Yes. FDA refused 3 shipment lines from Vemedia on June 3, 2019. The most recent, on June 3, 2019, was vitamin c (ascorbic acid), charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Vemedia's shipments?
- The most frequent charge is NO ENGLISH (required label information not in english, 3 lines).
- What is Vemedia's FEI number?
- Vemedia's FDA Establishment Identifier (FEI) is 3015341006.
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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.