FDA inspection

Shandong Lukang Shelile Pharmaceutical Co., Ltd.: FDA inspection ending Apr 30, 2026

FDA inspection 1320030 · No Action Indicated (NAI) · Jining

Key facts

Inspection ID 1320030
Firm Shandong Lukang Shelile Pharmaceutical Co., Ltd.
FEI number 3001040579
Address Zoucheng Industrial Park, 50 Hualu Road; Zoucheng
City Jining
Country China
Fiscal year 2026
Inspection end date Apr 30, 2026
Classification No Action Indicated (NAI)
Project area Pre-Approval Eval. of Animal Drugs and Food Additives
Product type Veterinary

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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