Tsin Tsin Food Ind. Corp. (Changhwa First Factory)
FDA import alert and refusal historyChang-Hua, TaiwanFEI 14568
As of October 26, 2026, Tsin Tsin Food Ind. Corp. (Changhwa First Factory) (Chang-Hua, Taiwan) is on the red list of FDA Import Alert 99-37 (Low-acid canned/acidified foods without scheduled process) for grass jelly drink beverage base; grass jelly, published by FDA on June 3, 2014, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-37 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Tsin Tsin Food Ind. Corp. (Changhwa First Factory)
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-37red listGrass Jelly Drink Beverage Base; GRASS JELLYSource
Questions about Tsin Tsin Food Ind. Corp. (Changhwa First Factory)
- Is Tsin Tsin Food Ind. Corp. (Changhwa First Factory) on an FDA import alert?
- Yes. As of October 26, 2026, Tsin Tsin Food Ind. Corp. (Changhwa First Factory) is on the red list of FDA Import Alert 99-37, “Low-acid canned/acidified foods without scheduled process”, for grass jelly drink beverage base; grass jelly; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from Tsin Tsin Food Ind. Corp. (Changhwa First Factory)?
- No FDA import refusals for Tsin Tsin Food Ind. Corp. (Changhwa First Factory) appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Tsin Tsin Food Ind. Corp. (Changhwa First Factory)'s FEI number?
- Tsin Tsin Food Ind. Corp. (Changhwa First Factory)'s FDA Establishment Identifier (FEI) is 14568.
- Can shipments from Tsin Tsin Food Ind. Corp. (Changhwa First Factory) still enter the U.S.?
- Shipments of grass jelly drink beverage base; grass jelly from Tsin Tsin Food Ind. Corp. (Changhwa First Factory) can be detained without physical examination under Import Alert 99-37; 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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