FDA Inspection 1253125 — Zhejiang Bamboo Pharmaceuticals Co., Ltd.

Zhejiang Bamboo Pharmaceuticals Co., Ltd. — FEI 3019684157

The FDA completed an inspection of Zhejiang Bamboo Pharmaceuticals Co., Ltd. on Sep 27, 2024 in Shaoxing. 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 27, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Shaoxing (China)