Hebei Anguo Pharmaceuticals Group Co., Ltd.
FDA import alert and refusal historyAnguo City, ChinaFEI 3005178023
As of October 26, 2026, Hebei Anguo Pharmaceuticals Group Co., Ltd. (Anguo City, China) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for herbals & botanical teas, n.e.c., published by FDA on September 18, 2009, 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 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Hebei Anguo Pharmaceuticals Group Co., Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listHerbals & Botanical Teas, N.E.C.Source
Questions about Hebei Anguo Pharmaceuticals Group Co., Ltd.
- Is Hebei Anguo Pharmaceuticals Group Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Hebei Anguo Pharmaceuticals Group Co., Ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for herbals & botanical teas, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Hebei Anguo Pharmaceuticals Group Co., Ltd.?
- No FDA import refusals for Hebei Anguo Pharmaceuticals Group Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Hebei Anguo Pharmaceuticals Group Co., Ltd.'s FEI number?
- Hebei Anguo Pharmaceuticals Group Co., Ltd.'s FDA Establishment Identifier (FEI) is 3005178023.
- Can shipments from Hebei Anguo Pharmaceuticals Group Co., Ltd. still enter the U.S.?
- Shipments of herbals & botanical teas, n.e.c. from Hebei Anguo Pharmaceuticals Group 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).
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