FDA inspection

Guangzhou Klarity Medical & Equipment Co.: FDA inspection ending Apr 20, 2016

FDA inspection 975308 · No Action Indicated (NAI) · Guangzhou

Key facts

Inspection ID 975308
Firm Guangzhou Klarity Medical & Equipment Co.
FEI number 3003803149
Address Meixingang & Zhongshan Rd.
City Guangzhou
Country China
Fiscal year 2016
Inspection end date Apr 20, 2016
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

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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