FDA inspection

Shenzhen Bi-Rich Medical Devices Co., Ltd: FDA inspection ending Nov 15, 2017

FDA inspection 1034058 · No Action Indicated (NAI) · Shenzhen

Key facts

Inspection ID 1034058
Firm Shenzhen Bi-Rich Medical Devices Co., Ltd
FEI number 3011716786
Address No. 10 Hongtianlu, Baoan
City Shenzhen
Country China
Fiscal year 2018
Inspection end date Nov 15, 2017
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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