FDA Inspection 1072549 — Xiamen LP Pharmaceutical Co., Ltd.

Xiamen LP Pharmaceutical Co., Ltd. — FEI 3013002864

The FDA completed an inspection of Xiamen LP Pharmaceutical Co., Ltd. on Nov 16, 2018 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
Nov 16, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Xia Men (China)