FDA inspection

Danyang Kawaza Medical Products Co., Ltd: FDA inspection ending Dec 4, 2014

FDA inspection 908745 · Voluntary Action Indicated (VAI) · Danyang City

Key facts

Inspection ID 908745
Firm Danyang Kawaza Medical Products Co., Ltd
FEI number 3005720080
Address No. 8 Shengchang West Road, Economy Development Zone
City Danyang City
Country China
Fiscal year 2015
Inspection end date Dec 4, 2014
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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