Sichuan Neo-Green Pharmaceutical Technology Development Co.
FDA import alert and refusal historyJinniu District, ChinaFEI 3010692630
As of October 26, 2026, Sichuan Neo-Green Pharmaceutical Technology Development Co. (Jinniu District, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for shan yao (chinese yam), published by FDA on March 13, 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 Sichuan Neo-Green Pharmaceutical Technology Development Co.
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-08red listShan Yao (Chinese Yam)Source
Questions about Sichuan Neo-Green Pharmaceutical Technology Development Co.
- Is Sichuan Neo-Green Pharmaceutical Technology Development Co. on an FDA import alert?
- Yes. As of October 26, 2026, Sichuan Neo-Green Pharmaceutical Technology Development Co. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for shan yao (chinese yam); FDA published the listing on March 13, 2014.
- Has FDA refused shipments from Sichuan Neo-Green Pharmaceutical Technology Development Co.?
- No FDA import refusals for Sichuan Neo-Green Pharmaceutical Technology Development Co. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Sichuan Neo-Green Pharmaceutical Technology Development Co.'s FEI number?
- Sichuan Neo-Green Pharmaceutical Technology Development Co.'s FDA Establishment Identifier (FEI) is 3010692630.
- Can shipments from Sichuan Neo-Green Pharmaceutical Technology Development Co. still enter the U.S.?
- Shipments of shan yao (chinese yam) from Sichuan Neo-Green Pharmaceutical Technology Development Co. 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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