SupplierRadar

Myanmar Oasis Manufacturing Co.,Ltd.

FDA import alert and refusal historyDagon Seikkan, MyanmarFEI 3021479716

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Myanmar Oasis Manufacturing Co.,Ltd..

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectMyanmar Oasis Manufacturing Co.,Ltd added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 26, 2026, Myanmar Oasis Manufacturing Co.,Ltd. (Dagon Seikkan, Myanmar) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for royal d electrolyte beverage, published by FDA on September 14, 2023, and has 1 FDA import refusal recorded since October 2016.

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

Current status

Last import refusal
Soft drink, cola, carbonated · UNSAFE COL
Last warning letter
None found
Last inspection
None on record

Every FDA record for Myanmar Oasis Manufacturing Co.,Ltd.

2 records, newest first. Each line links to the FDA page it came from.

2023

  1. Import refusal
    Refused, Soft drink, cola, carbonatedUNSAFE COLNO ENGLISHYELLOW #5Entry AC1-6535634-9
    Source
  2. Import alert listing
    Listed on Import Alert 45-02red listRoyal d electrolyte beverage
    Source

Refusal charges, in plain English

  • NO ENGLISH1 refused line

    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.

  • UNSAFE COL1 refused line

    Color additive unsafe under section 721

    The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

  • YELLOW #51 refused line

    FD&C Yellow No. 5 not declared

    The food appeared to contain the color additive FD&C Yellow No. 5 without declaring it on the label as 21 CFR 74.705 requires.

Questions about Myanmar Oasis Manufacturing Co.,Ltd.

Is Myanmar Oasis Manufacturing Co.,Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Myanmar Oasis Manufacturing Co.,Ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for royal d electrolyte beverage; FDA published the listing on September 14, 2023.
Has FDA refused shipments from Myanmar Oasis Manufacturing Co.,Ltd.?
Yes. FDA refused 1 shipment line from Myanmar Oasis Manufacturing Co.,Ltd. on November 21, 2023. The most recent, on November 21, 2023, was soft drink, cola, carbonated, charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Myanmar Oasis Manufacturing Co.,Ltd.'s shipments?
The most frequent charges are NO ENGLISH (required label information not in english, 1 line) and UNSAFE COL (color additive unsafe under section 721, 1 line).
What is Myanmar Oasis Manufacturing Co.,Ltd.'s FEI number?
Myanmar Oasis Manufacturing Co.,Ltd.'s FDA Establishment Identifier (FEI) is 3021479716.
Can shipments from Myanmar Oasis Manufacturing Co.,Ltd. still enter the U.S.?
Shipments of royal d electrolyte beverage from Myanmar Oasis Manufacturing Co.,Ltd. can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

Buying from Myanmar Oasis Manufacturing Co.,Ltd.?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Myanmar Oasis Manufacturing Co.,Ltd..

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectMyanmar Oasis Manufacturing Co.,Ltd added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

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.