FDA inspection

Airflo (Xiamen) Medical Company, Limited: FDA inspection ending May 7, 2015

FDA inspection 932154 · Voluntary Action Indicated (VAI) · Xiamen

Key facts

Inspection ID 932154
Firm Airflo (Xiamen) Medical Company, Limited
FEI number 3008957229
Address Haijingdonglu F 4, No. 6 Haijingdonglu; Haicang
City Xiamen
Country China
Fiscal year 2015
Inspection end date May 7, 2015
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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