FDA inspection

COMBO (ZHONG SHAN) MEDICAL EQUIPMENT CO., LTD.: FDA inspection ending Dec 16, 2015

FDA inspection 953488 · No Action Indicated (NAI) · ZHONGSHAN CITY

Key facts

Inspection ID 953488
Firm COMBO (ZHONG SHAN) MEDICAL EQUIPMENT CO., LTD.
FEI number 3007222468
Address THE REARWARD OF BUILDING NO. 83, YUMIN R, DONGSHENG TOWN
City ZHONGSHAN CITY
Country China
Fiscal year 2016
Inspection end date Dec 16, 2015
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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