FDA inspection

NINGBO KANGMAILONG MEDICAL APARATUS CO LTD: FDA inspection ending Sep 27, 2012

FDA inspection 802682 · No Action Indicated (NAI) · Ningbo

Key facts

Inspection ID 802682
Firm NINGBO KANGMAILONG MEDICAL APARATUS CO LTD
FEI number 3006891315
Address NO. 381 XINJIANG ROAD
City Ningbo
Country China
Fiscal year 2012
Inspection end date Sep 27, 2012
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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