FDA inspection

Zhongfu Pharmaceutical Co., Ltd.: FDA inspection ending Sep 28, 2012

FDA inspection 802551 · No Action Indicated (NAI) · Weifang

Key facts

Inspection ID 802551
Firm Zhongfu Pharmaceutical Co., Ltd.
FEI number 3002808105
Address No. 2709 Yuwang North Street, Hanting District
City Weifang
Country China
Fiscal year 2012
Inspection end date Sep 28, 2012
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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