Qinghai Baojiantang Pharmaceutical Co., Ltd
FDA import alert and refusal historyQinghai, ChinaFEI 3010900590
As of October 26, 2026, Qinghai Baojiantang Pharmaceutical Co., Ltd (Qinghai, China) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for male sexual stimulant- u.s.a. wolf brother strong man, published by FDA on September 25, 2015, 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 54-16 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Qinghai Baojiantang Pharmaceutical Co., Ltd
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 54-16red listMale Sexual Stimulant- U.S.A. Wolf Brother Strong ManSource
Questions about Qinghai Baojiantang Pharmaceutical Co., Ltd
- Is Qinghai Baojiantang Pharmaceutical Co., Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Qinghai Baojiantang Pharmaceutical Co., Ltd is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for male sexual stimulant- u.s.a. wolf brother strong man; FDA published the listing on September 25, 2015.
- Has FDA refused shipments from Qinghai Baojiantang Pharmaceutical Co., Ltd?
- No FDA import refusals for Qinghai Baojiantang Pharmaceutical Co., Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Qinghai Baojiantang Pharmaceutical Co., Ltd's FEI number?
- Qinghai Baojiantang Pharmaceutical Co., Ltd's FDA Establishment Identifier (FEI) is 3010900590.
- Can shipments from Qinghai Baojiantang Pharmaceutical Co., Ltd still enter the U.S.?
- Shipments of male sexual stimulant- u.s.a. wolf brother strong man from Qinghai Baojiantang Pharmaceutical Co., Ltd can be detained without physical examination under Import Alert 54-16; 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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