FDA Inspection 1067628 — Changzhou Ruiming Pharmaceuticals Co. Ltd.

Changzhou Ruiming Pharmaceuticals Co. Ltd. — FEI 3007086821

The FDA completed an inspection of Changzhou Ruiming Pharmaceuticals Co. Ltd. on Sep 13, 2018 in Changzhou. 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)
End Date
Sep 13, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Changzhou (China)