FDA Inspection 1239875 — Xiamen LP Pharmaceutical Co., Ltd.

Xiamen LP Pharmaceutical Co., Ltd. — FEI 3013002864

The FDA completed an inspection of Xiamen LP Pharmaceutical Co., Ltd. on Apr 19, 2024 in Xia Men. 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
Apr 19, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Xia Men (China)