FDA Inspection 852982 — Chongqing Lummy Pharmaceutical Co. Ltd.

Chongqing Lummy Pharmaceutical Co. Ltd. — FEI 3006560479

The FDA completed an inspection of Chongqing Lummy Pharmaceutical Co. Ltd. on July 10, 2013 in Chongqing. 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
July 10, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chongqing (China)