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FDA Inspection 1080590 — 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 December 14, 2018 in Jining. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 14, 2018
Fiscal Year
2019
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))
  • 1274884 (VAI Fri May 30 2025 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