FDA Inspection 925759 — Changzhou Sunlight Pharmaceutical Co., Ltd.

Changzhou Sunlight Pharmaceutical Co., Ltd. — FEI 3003662818

The FDA completed an inspection of Changzhou Sunlight Pharmaceutical Co., Ltd. on April 10, 2015 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) (VAI)
End Date
April 10, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Changzhou (China)