FDA inspection

Shandong Xinhua Pharmaceutical Co., Ltd. First Plant: FDA inspection ending Mar 31, 2016

FDA inspection 1000050 · No Action Indicated (NAI) · Zibo

Key facts

Inspection ID 1000050
Firm Shandong Xinhua Pharmaceutical Co., Ltd. First Plant
FEI number 3002808153
Address 14 Dongyi Road, Zhangdian District
City Zibo
Country China
Fiscal year 2016
Inspection end date Mar 31, 2016
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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