FDA Inspection 1241747 — Zhongfu Pharmaceutical Co., Ltd.

Zhongfu Pharmaceutical Co., Ltd. — FEI 3002808105

The FDA completed an inspection of Zhongfu Pharmaceutical Co., Ltd. on May 24, 2024 in Weifang. 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
May 24, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Weifang (China)