FDA inspection

SunMed AP, Ltd.: FDA inspection ending May 30, 2013

FDA inspection 843271 · No Action Indicated (NAI) · Zhuhai

Key facts

Inspection ID 843271
Firm SunMed AP, Ltd.
FEI number 3005998497
Address Qianwu Industry Park, Doume District
City Zhuhai
Country China
Fiscal year 2013
Inspection end date May 30, 2013
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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