FDA inspection

Shenzhen Coreray Technology Co., Ltd.: FDA inspection ending Aug 6, 2024

FDA inspection 1249765 · No Action Indicated (NAI) · Shenzhen

Key facts

Inspection ID 1249765
Firm Shenzhen Coreray Technology Co., Ltd.
FEI number 3014233600
Address Jingxuan Park 5th Floor, 2 Nd Donghuan Road; Longhuazhen Longgang
City Shenzhen
Country China
Fiscal year 2024
Inspection end date Aug 6, 2024
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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