FDA inspection

Shandong Lukang Shelile Pharmaceutical Co., Ltd.: FDA inspection ending Dec 5, 2013

FDA inspection 865966 · No Action Indicated (NAI) · Jining

Key facts

Inspection ID 865966
Firm Shandong Lukang Shelile Pharmaceutical Co., Ltd.
FEI number 3001040579
Address Zoucheng Industrial Park, 50 Hualu Road
City Jining
Country China
Fiscal year 2014
Inspection end date Dec 5, 2013
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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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