Golden Crow Shwe Kyee · 99-39 · BURMA (MYANMAR)
For Golden Crow Shwe Kyee, import alert is 99-39; country is BURMA (MYANMAR); import alert name is Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded; product is Special Dried Butter Cake; product code is 03 R - - 01 Cake Without Custard or Cream Filling; date published is 03/15/2018; address is 282 Magway St. Ind. Zone, Ward 23. S. , Rangoon, Rangoon BURMA (MYANMAR), verified against its source on 2026-09-30.
- Firm
- Golden Crow Shwe Kyee verified
- Import alert
- 99-39
- Import alert name
- Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded
- Country
- BURMA (MYANMAR) verified
- Address
- 282 Magway St. Ind. Zone, Ward 23. S. , Rangoon, Rangoon BURMA (MYANMAR) verified
- Date published
- 03/15/2018 verified
- Product code
- 03 R - - 01 Cake Without Custard or Cream Filling verified
- Product
- Special Dried Butter Cake verified
- FDA notes
- Section 403 (i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient; Section 403(f) of the FD&C Act in that the label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2) verified
What the source says
Golden Crow Shwe Kyee Date Published : 03/15/2018 282 Magway St. Ind. Zone, Ward 23. S. , Rangoon, Rangoon BURMA (MYANMAR)
— accessdata.fda.gov, retrieved 2026-09-15
Where each value comes from
The values above are stated away from the sentence quoted with the answer, so the passage that states them is shown here too.
Product code, Product and FDA notes
03 R - - 01 Cake Without Custard or Cream Filling Date Published: 03/15/2018 Desc: Special Dried Butter Cake Notes: Section 403 (i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient; Section 403(f) of the FD&C Act in that the label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2)
— all from accessdata.fda.gov, retrieved 2026-09-15
Source
- accessdata.fda.govhttps://www.accessdata.fda.gov/cms_ia/importalert_1144.html
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