FDA Inspection 1219460 — Chengdu Shengnuo Biopharm Co., Ltd.

Chengdu Shengnuo Biopharm Co., Ltd. — FEI 3006257504

The FDA completed an inspection of Chengdu Shengnuo Biopharm Co., Ltd. on September 8, 2023 in Chengdu. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 8, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chengdu (China)