# Zhejiang Qianfei Enterprise Co. Ltd. · 66-40 · CHINA — FDA import alert red lists: firms subject to detention without physical examination For Zhejiang Qianfei Enterprise Co. Ltd. · 66-40 · CHINA, import alert is 66-40; import alert name is "Detention Without Physical Examination of Drugs From Firms Which Have Not Met Drug GMPs"; country is CHINA; product code is 55 - - - -- Pharm Necess & Ctnr For Drug/Bio | 58 - - - -- Human and Animal Therapeutic Biologic and Biosimilar Drugs | 60 - - - -- Human and Animal Drugs | 61 - - - -- Human and Animal Drugs | 62 - - - -- Human and Animal Drugs | 63 - - - -- Human and Animal Drugs | 64 - - - -- Human and Animal Drugs | 65 - - - -- Human and Animal Drugs | 66 - - - -- Human and Animal Drugs; date published is 11/24/2015; address is No 173 Wulian Road , Yiwu , Jinhua, Zhejiang CHINA, verified against its source on 2026-09-16. - **Firm:** Zhejiang Qianfei Enterprise Co. Ltd. _(verified: appears in the quote below)_ - **Import alert:** 66-40 - **Import alert name:** "Detention Without Physical Examination of Drugs From Firms Which Have Not Met Drug GMPs" - **Country:** CHINA _(verified: appears in the quote below)_ - **Address:** No 173 Wulian Road , Yiwu , Jinhua, Zhejiang CHINA _(verified: appears in the quote below)_ - **Date published:** 11/24/2015 _(verified: appears in the quote below)_ - **Product code:** 55 - - - -- Pharm Necess & Ctnr For Drug/Bio | 58 - - - -- Human and Animal Therapeutic Biologic and Biosimilar Drugs | 60 - - - -- Human and Animal Drugs | 61 - - - -- Human and Animal Drugs | 62 - - - -- Human and Animal Drugs | 63 - - - -- Human and Animal Drugs | 64 - - - -- Human and Animal Drugs | 65 - - - -- Human and Animal Drugs | 66 - - - -- Human and Animal Drugs _(verified: each item appears in the quote below)_ - **FDA notes:** All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices | All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices | All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices | All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices | All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices | All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices | All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices | All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices _(verified: each item appears in the quote below)_ ## What the source says > Zhejiang Qianfei Enterprise Co. Ltd. Date Published : 11/24/2015 No 173 Wulian Road , Yiwu , Jinhua, Zhejiang CHINA 55 - - - -- Pharm Necess & Ctnr For Drug/Bio Date Published: 11/24/2015 Notes: All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices 58 - - - -- Human and Animal Therapeutic Biologic and Biosimilar Drugs Date Published: 05/26/2022 60 - - - -- Human and Animal Drugs Date Published: 11/24/2015 Notes: All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices 61 - - - -- Human and Animal Drugs Date Published: 11/24/2015 Notes: All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices 62 - - - -- Human and Animal Drugs Date Published: 11/24/2015 Notes: All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices 63 - - - -- Human and Animal Drugs Date Published: 11/24/2015 Notes: All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices 64 - - - -- Human and Animal Drugs Date Published: 11/24/2015 Notes: All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices 65 - - - -- Human and Animal Drugs Date Published: 11/24/2015 Notes: All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices 66 - - - -- Human and Animal Drugs Date Published: 11/24/2015 Notes: All Drug and Drug Products; Problems: (GMP) Good Manufacturing Practices ## Source - https://www.accessdata.fda.gov/cms_ia/importalert_189.html Last verified: 2026-09-16. Review by: 2026-11-15. Part of [FDA import alert red lists: firms subject to detention without physical examination](https://referencesource.org/fda-import-alert-red-list/).