Jinzhou Rongjin Health Care Products Company Limited
FDA import alert and refusal historyJinzhou, ChinaFEI 3004397663
Recorded by FDA as JINZHOU RONGJIN HEALTH CARE PRODUCTS COMPANY LIMITED
As of October 27, 2026, Jinzhou Rongjin Health Care Products Company Limited (Jinzhou, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for ginseng radix rubra, published by FDA on September 16, 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 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 Jinzhou Rongjin Health Care Products Company Limited
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listGinseng Radix RubraSource
Questions about Jinzhou Rongjin Health Care Products Company Limited
- Is Jinzhou Rongjin Health Care Products Company Limited on an FDA import alert?
- Yes. As of October 27, 2026, Jinzhou Rongjin Health Care Products Company Limited is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for ginseng radix rubra; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Jinzhou Rongjin Health Care Products Company Limited?
- No FDA import refusals for Jinzhou Rongjin Health Care Products Company Limited appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Jinzhou Rongjin Health Care Products Company Limited's FEI number?
- Jinzhou Rongjin Health Care Products Company Limited's FDA Establishment Identifier (FEI) is 3004397663.
- Can shipments from Jinzhou Rongjin Health Care Products Company Limited still enter the U.S.?
- Shipments of ginseng radix rubra from Jinzhou Rongjin Health Care Products Company Limited 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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