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FDA Inspection 619046 — Shandong Lukang Shelile Pharmaceutical Co., Ltd.

Shandong Lukang Shelile Pharmaceutical Co., Ltd. — FEI 3001040579

The FDA completed an inspection of Shandong Lukang Shelile Pharmaceutical Co., Ltd. on July 30, 2009 in Jining. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 30, 2009
Fiscal Year
2009
Product Type
Veterinary
Project Area
Pre-Approval Eval. of Animal Drugs and Food Additives
Location
Jining (China)

Facility

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FDA data resources