Shandong Medicines & Health Products Imp & Exp Co.
FDA import alert and refusal historyQingdao, ChinaFEI 3005129946
Recorded by FDA as SHANDONG MEDICINES & HEALTH PRODUCTS IMP & EXP CO.
As of October 26, 2026, Shandong Medicines & Health Products Imp & Exp Co. (Qingdao, China) is on the red list of FDA Import Alert 99-46 (Imported human foods: filth) for white garlic bulbs, published by FDA on May 18, 2022, 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 99-46 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Shandong Medicines & Health Products Imp & Exp Co.
1 record, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 99-46red listWhite garlic bulbsSource
Questions about Shandong Medicines & Health Products Imp & Exp Co.
- Is Shandong Medicines & Health Products Imp & Exp Co. on an FDA import alert?
- Yes. As of October 26, 2026, Shandong Medicines & Health Products Imp & Exp Co. is on the red list of FDA Import Alert 99-46, “Imported human foods: filth”, for white garlic bulbs; FDA published the listing on May 18, 2022.
- Has FDA refused shipments from Shandong Medicines & Health Products Imp & Exp Co.?
- No FDA import refusals for Shandong Medicines & Health Products Imp & Exp Co. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Shandong Medicines & Health Products Imp & Exp Co.'s FEI number?
- Shandong Medicines & Health Products Imp & Exp Co.'s FDA Establishment Identifier (FEI) is 3005129946.
- Can shipments from Shandong Medicines & Health Products Imp & Exp Co. still enter the U.S.?
- Shipments of white garlic bulbs from Shandong Medicines & Health Products Imp & Exp Co. can be detained without physical examination under Import Alert 99-46; 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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