Holy Garden Company Limited
FDA import alert and refusal historyYangon, MyanmarFEI 3013615733
Recorded by FDA as HOLY GARDEN COMPANY LIMITED
As of October 26, 2026, Holy Garden Company Limited (Yangon, Myanmar) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for hilsa shad, published by FDA on November 20, 2017, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-81 · red list
- Last import refusal
- Herring · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Holy Garden Company Limited
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, HerringSALMONELLAEntry W04-0069209-5Source
- Import alert listingListed on Import Alert 16-81red listHilsa ShadSource
Refusal charges, in plain English
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Holy Garden Company Limited
- Is Holy Garden Company Limited on an FDA import alert?
- Yes. As of October 26, 2026, Holy Garden Company Limited is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for hilsa shad; FDA published the listing on November 20, 2017.
- Has FDA refused shipments from Holy Garden Company Limited?
- Yes. FDA refused 1 shipment line from Holy Garden Company Limited on November 28, 2017. The most recent, on November 28, 2017, was herring, charged as SALMONELLA (salmonella).
- Why did FDA refuse Holy Garden Company Limited's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Holy Garden Company Limited's FEI number?
- Holy Garden Company Limited's FDA Establishment Identifier (FEI) is 3013615733.
- Can shipments from Holy Garden Company Limited still enter the U.S.?
- Shipments of hilsa shad from Holy Garden Company Limited can be detained without physical examination under Import Alert 16-81; 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).
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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.