China GuangDong FoShan City NanHai Peng Yang T.C.M. Co. Ltd.
FDA import alert and refusal historyFoshan, ChinaFEI 3004324427
As of October 27, 2026, China GuangDong FoShan City NanHai Peng Yang T.C.M. Co. Ltd. (Foshan, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for phnax notoginseng, published by FDA on June 18, 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for China GuangDong FoShan City NanHai Peng Yang T.C.M. Co. Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-08red listPhnax NotoginsengSource
Questions about China GuangDong FoShan City NanHai Peng Yang T.C.M. Co. Ltd.
- Is China GuangDong FoShan City NanHai Peng Yang T.C.M. Co. Ltd. on an FDA import alert?
- Yes. As of October 27, 2026, China GuangDong FoShan City NanHai Peng Yang T.C.M. Co. Ltd. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for phnax notoginseng; FDA published the listing on June 18, 2014.
- Has FDA refused shipments from China GuangDong FoShan City NanHai Peng Yang T.C.M. Co. Ltd.?
- No FDA import refusals for China GuangDong FoShan City NanHai Peng Yang T.C.M. Co. Ltd. appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is China GuangDong FoShan City NanHai Peng Yang T.C.M. Co. Ltd.'s FEI number?
- China GuangDong FoShan City NanHai Peng Yang T.C.M. Co. Ltd.'s FDA Establishment Identifier (FEI) is 3004324427.
- Can shipments from China GuangDong FoShan City NanHai Peng Yang T.C.M. Co. Ltd. still enter the U.S.?
- Shipments of phnax notoginseng from China GuangDong FoShan City NanHai Peng Yang T.C.M. Co. Ltd. can be detained without physical examination under Import Alert 99-08; 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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