FDA inspection

Novo Nordisk Pharmaceuticals Co. Ltd: FDA inspection ending Nov 2, 2017

FDA inspection 1032345 · No Action Indicated (NAI) · Tianjin

Key facts

Inspection ID 1032345
Firm Novo Nordisk Pharmaceuticals Co. Ltd
FEI number 3005186124
Address 99 Nanhailu, Tanggueconomic Technological Development
City Tianjin
Country China
Fiscal year 2018
Inspection end date Nov 2, 2017
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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