FDA Inspection 1069379 — Wuhan Biocause Pharmaceutical Development Co., Ltd.

Wuhan Biocause Pharmaceutical Development Co., Ltd. — FEI 3004202226

The FDA completed an inspection of Wuhan Biocause Pharmaceutical Development Co., Ltd. on August 24, 2018 in Wuhan. 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
August 24, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wuhan (China)