FDA inspection

Shandong Lukang Shelile Pharmaceutical Co., Ltd.: FDA inspection ending May 30, 2025

FDA inspection 1274884 · Voluntary Action Indicated (VAI) · Jining

Key facts

Inspection ID 1274884
Firm Shandong Lukang Shelile Pharmaceutical Co., Ltd.
FEI number 3001040579
Address Hualu Road, Zoucheng Industrial Park 50
City Jining
Country China
Fiscal year 2025
Inspection end date May 30, 2025
Classification Voluntary Action Indicated (VAI)
Project area Monitoring of Marketed Animal Drugs, Feed, and Devices
Product type Veterinary

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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