FDA Inspection 1254530 — Sinopep-Allsino Biopharmaceutical Co., Ltd.

Sinopep-Allsino Biopharmaceutical Co., Ltd. — FEI 3005460102

The FDA completed an inspection of Sinopep-Allsino Biopharmaceutical Co., Ltd. on Sep 20, 2024 in Lianyungang. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 20, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lianyungang (China)