FDA inspection

Shandong Lukang Shelile Pharmaceutical Co., Ltd.: FDA inspection ending Nov 6, 2015

FDA inspection 953818 · No Action Indicated (NAI) · Jining

Key facts

Inspection ID 953818
Firm Shandong Lukang Shelile Pharmaceutical Co., Ltd.
FEI number 3001040579
Address Zoucheng Industrial Park, 50 Hualu Road
City Jining
Country China
Fiscal year 2016
Inspection end date Nov 6, 2015
Classification No Action Indicated (NAI)
Project area Monitoring of Marketed Animal Drugs, Feed, and Devices
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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