CV Mutiara Madu Kuansing
FDA import alert and refusal historyTeluk Kuantan, IndonesiaFEI 3015301477
Recorded by FDA as CV MUTIARA MADU KUANSING
As of October 26, 2026, CV Mutiara Madu Kuansing is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 1, 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
- Honey · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for CV Mutiara Madu Kuansing
1 record, newest first. Each line links to the FDA page it came from.
2019
- Import refusalRefused, HoneyUNAPPROVEDEntry AEK-6355080-7Source
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 CV Mutiara Madu Kuansing
- Is CV Mutiara Madu Kuansing on an FDA import alert?
- No listing for CV Mutiara Madu Kuansing appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Indonesia page.
- Has FDA refused shipments from CV Mutiara Madu Kuansing?
- Yes. FDA refused 1 shipment line from CV Mutiara Madu Kuansing on October 1, 2019. The most recent, on October 1, 2019, was honey, charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse CV Mutiara Madu Kuansing's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is CV Mutiara Madu Kuansing's FEI number?
- CV Mutiara Madu Kuansing's FDA Establishment Identifier (FEI) is 3015301477.
Buying from CV Mutiara Madu Kuansing?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.