Tai Ying Co., Ltd.
FDA import alert and refusal historyTai Zhong Shi, TaiwanFEI 3013280753
As of October 26, 2026, Tai Ying Co., Ltd. (Tai Zhong Shi, Taiwan) is on the red list of FDA Import Alert 20-07 (Juice from processors not in compliance with juice HACCP) for pasteurized and frozen fruit juices, published by FDA on October 20, 2026, 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 20-07 · red list
- Last import refusal
- Lemon, citrus fruit juices or concentrates · ADDED BULK
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Tai Ying Co., Ltd.
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 20-07red listPasteurized and Frozen Fruit JuicesSource
2025
- Import refusalRefused, Lemon, citrus fruit juices or concentratesADDED BULKEntry T81-0223522-3Source
Refusal charges, in plain English
- ADDED BULK1 refused line
ADDED BULK
Questions about Tai Ying Co., Ltd.
- Is Tai Ying Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Tai Ying Co., Ltd. is on the red list of FDA Import Alert 20-07, “Juice from processors not in compliance with juice HACCP”, for pasteurized and frozen fruit juices; FDA published the listing on October 20, 2026.
- Has FDA refused shipments from Tai Ying Co., Ltd.?
- Yes. FDA refused 1 shipment line from Tai Ying Co., Ltd. on December 17, 2025. The most recent, on December 17, 2025, was lemon, citrus fruit juices or concentrates, charged as ADDED BULK (added bulk).
- Why did FDA refuse Tai Ying Co., Ltd.'s shipments?
- The most frequent charge is ADDED BULK (added bulk, 1 line).
- What is Tai Ying Co., Ltd.'s FEI number?
- Tai Ying Co., Ltd.'s FDA Establishment Identifier (FEI) is 3013280753.
- Can shipments from Tai Ying Co., Ltd. still enter the U.S.?
- Shipments of pasteurized and frozen fruit juices from Tai Ying Co., Ltd. can be detained without physical examination under Import Alert 20-07; 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.