East Asia Laboratories Inc
FDA import alert and refusal historySan Mateo Rizal, MalaysiaFEI 3012084257
As of October 26, 2026, East Asia Laboratories Inc is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on June 21, 2022, 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 c (ascorbic acid) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for East Asia Laboratories Inc
3 records, newest first. Each line links to the FDA page it came from.
2022
- Import refusalSource
Refused, 3 lines in one entry: Vitamin c (ascorbic acid); Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. and 1 moreUNAPPROVEDEntry AEK-1257055-0Show 3 linesHide lines
- Refused, Vitamin c (ascorbic acid)UNAPPROVEDEntry AEK-1257055-0Source
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry AEK-1257055-0Source
- Refused, Pantothenic acid (panthenol) (vitamin)UNAPPROVEDEntry AEK-1257055-0Source
Refusal charges, in plain English
- UNAPPROVED3 refused lines
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 East Asia Laboratories Inc
- Is East Asia Laboratories Inc on an FDA import alert?
- No listing for East Asia Laboratories Inc appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Malaysia page.
- Has FDA refused shipments from East Asia Laboratories Inc?
- Yes. FDA refused 3 shipment lines from East Asia Laboratories Inc on June 21, 2022. The most recent, on June 21, 2022, was vitamin c (ascorbic acid), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse East Asia Laboratories Inc's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 3 lines).
- What is East Asia Laboratories Inc's FEI number?
- East Asia Laboratories Inc's FDA Establishment Identifier (FEI) is 3012084257.
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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.