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FDA Inspection 1274884 — 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 May 30, 2025 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
May 30, 2025
Fiscal Year
2025
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Jining (China)

Facility

Other inspections at this facility

  • 1320030 (NAI Thu Apr 30 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1080590 (NAI Fri Dec 14 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 953818 (NAI Fri Nov 06 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 865966 (NAI Thu Dec 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 619046 (VAI Thu Jul 30 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources